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esv2761932

  • Variant Calls:37
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:25,579

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 516 SVs from 66 studies. See in: genome view    
Remapped(Score: Perfect):97,264,844-97,290,422Question Mark
Overlapping variant regions from other studies: 516 SVs from 66 studies. See in: genome view    
Remapped(Score: Perfect):97,808,074-97,833,652Question Mark
Overlapping variant regions from other studies: 245 SVs from 22 studies. See in: genome view    
Submitted genomic95,609,078-95,634,656Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartOuter Stop
esv2761932RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000015.10Chr1597,264,84497,290,422
esv2761932RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1597,808,07497,833,652
esv2761932Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000015.8Chr1595,609,07895,634,656

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv7000425copy number lossSW_0716SNP arraySNP genotyping analysis37
essv7000426copy number lossSW_1020SNP arraySNP genotyping analysis32
essv7000427copy number lossSW_1246SNP arraySNP genotyping analysis37
essv7000428copy number lossSW_0820SNP arraySNP genotyping analysis34
essv7000429copy number lossSW_0172SNP arraySNP genotyping analysis45
essv7000430copy number lossSW_0189SNP arraySNP genotyping analysis53
essv7000431copy number lossSW_0199SNP arraySNP genotyping analysis34
essv7000432copy number lossSW_0203SNP arraySNP genotyping analysis49
essv7000434copy number lossSW_0640SNP arraySNP genotyping analysis30
essv7000435copy number lossSW_0883SNP arraySNP genotyping analysis37
essv7000436copy number lossSW_1012SNP arraySNP genotyping analysis39
essv7000437copy number lossSW_1163SNP arraySNP genotyping analysis45
essv7000438copy number lossSW_1189SNP arraySNP genotyping analysis35
essv7000439copy number lossSW_1193SNP arraySNP genotyping analysis39
essv7000440copy number lossSW_1294SNP arraySNP genotyping analysis32
essv7000441copy number lossSW_1346SNP arraySNP genotyping analysis42
essv7000442copy number lossSW_1405SNP arraySNP genotyping analysis39
essv7000443copy number lossSW_1476SNP arraySNP genotyping analysis44
essv7000445copy number lossSW_1510SNP arraySNP genotyping analysis42
essv7000446copy number lossSW_1520SNP arraySNP genotyping analysis36
essv7000447copy number lossSW_0009SNP arraySNP genotyping analysis48
essv7000448copy number lossSW_0017SNP arraySNP genotyping analysis34
essv7000449copy number lossSW_0045SNP arraySNP genotyping analysis39
essv7000450copy number lossSW_0060SNP arraySNP genotyping analysis39
essv7000451copy number lossSW_0086SNP arraySNP genotyping analysis50
essv7000452copy number lossSW_0100SNP arraySNP genotyping analysis38
essv7000453copy number lossSW_0341SNP arraySNP genotyping analysis25
essv7000454copy number lossSW_0625SNP arraySNP genotyping analysis41
essv7000456copy number lossSW_0786SNP arraySNP genotyping analysis48
essv7000457copy number lossSW_0890SNP arraySNP genotyping analysis55
essv7000458copy number lossSW_1045SNP arraySNP genotyping analysis49
essv7000459copy number lossSW_1046SNP arraySNP genotyping analysis32
essv7000460copy number lossSW_1105SNP arraySNP genotyping analysis49
essv7000461copy number lossSW_1113SNP arraySNP genotyping analysis51
essv7000462copy number lossSW_1162SNP arraySNP genotyping analysis54
essv7000463copy number lossSW_1175SNP arraySNP genotyping analysis45
essv7000464copy number lossSW_1242SNP arraySNP genotyping analysis35

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv7000425RemappedPerfectNC_000015.10:g.(?_
97264844)_(9729042
2_?)del
GRCh38.p12First PassNC_000015.10Chr1597,264,84497,290,422
essv7000426RemappedPerfectNC_000015.10:g.(?_
97264844)_(9729042
2_?)del
GRCh38.p12First PassNC_000015.10Chr1597,264,84497,290,422
essv7000427RemappedPerfectNC_000015.10:g.(?_
97264844)_(9729042
2_?)del
GRCh38.p12First PassNC_000015.10Chr1597,264,84497,290,422
essv7000428RemappedPerfectNC_000015.10:g.(?_
97274562)_(9728544
7_?)del
GRCh38.p12First PassNC_000015.10Chr1597,274,56297,285,447
essv7000429RemappedPerfectNC_000015.10:g.(?_
97274562)_(9728895
7_?)del
GRCh38.p12First PassNC_000015.10Chr1597,274,56297,288,957
essv7000430RemappedPerfectNC_000015.10:g.(?_
97274562)_(9728895
7_?)del
GRCh38.p12First PassNC_000015.10Chr1597,274,56297,288,957
essv7000431RemappedPerfectNC_000015.10:g.(?_
97274562)_(9728895
7_?)del
GRCh38.p12First PassNC_000015.10Chr1597,274,56297,288,957
essv7000432RemappedPerfectNC_000015.10:g.(?_
97274562)_(9728895
7_?)del
GRCh38.p12First PassNC_000015.10Chr1597,274,56297,288,957
essv7000434RemappedPerfectNC_000015.10:g.(?_
97274562)_(9728895
7_?)del
GRCh38.p12First PassNC_000015.10Chr1597,274,56297,288,957
essv7000435RemappedPerfectNC_000015.10:g.(?_
97274562)_(9728895
7_?)del
GRCh38.p12First PassNC_000015.10Chr1597,274,56297,288,957
essv7000436RemappedPerfectNC_000015.10:g.(?_
97274562)_(9728895
7_?)del
GRCh38.p12First PassNC_000015.10Chr1597,274,56297,288,957
essv7000437RemappedPerfectNC_000015.10:g.(?_
97274562)_(9728895
7_?)del
GRCh38.p12First PassNC_000015.10Chr1597,274,56297,288,957
essv7000438RemappedPerfectNC_000015.10:g.(?_
97274562)_(9728895
7_?)del
GRCh38.p12First PassNC_000015.10Chr1597,274,56297,288,957
essv7000439RemappedPerfectNC_000015.10:g.(?_
97274562)_(9728895
7_?)del
GRCh38.p12First PassNC_000015.10Chr1597,274,56297,288,957
essv7000440RemappedPerfectNC_000015.10:g.(?_
97274562)_(9728895
7_?)del
GRCh38.p12First PassNC_000015.10Chr1597,274,56297,288,957
essv7000441RemappedPerfectNC_000015.10:g.(?_
97274562)_(9728895
7_?)del
GRCh38.p12First PassNC_000015.10Chr1597,274,56297,288,957
essv7000442RemappedPerfectNC_000015.10:g.(?_
97274562)_(9728895
7_?)del
GRCh38.p12First PassNC_000015.10Chr1597,274,56297,288,957
essv7000443RemappedPerfectNC_000015.10:g.(?_
97274562)_(9728895
7_?)del
GRCh38.p12First PassNC_000015.10Chr1597,274,56297,288,957
essv7000445RemappedPerfectNC_000015.10:g.(?_
97274562)_(9728895
7_?)del
GRCh38.p12First PassNC_000015.10Chr1597,274,56297,288,957
essv7000446RemappedPerfectNC_000015.10:g.(?_
97274562)_(9728895
7_?)del
GRCh38.p12First PassNC_000015.10Chr1597,274,56297,288,957
essv7000447RemappedPerfectNC_000015.10:g.(?_
97274562)_(9729042
2_?)del
GRCh38.p12First PassNC_000015.10Chr1597,274,56297,290,422
essv7000448RemappedPerfectNC_000015.10:g.(?_
97274562)_(9729042
2_?)del
GRCh38.p12First PassNC_000015.10Chr1597,274,56297,290,422
essv7000449RemappedPerfectNC_000015.10:g.(?_
97274562)_(9729042
2_?)del
GRCh38.p12First PassNC_000015.10Chr1597,274,56297,290,422
essv7000450RemappedPerfectNC_000015.10:g.(?_
97274562)_(9729042
2_?)del
GRCh38.p12First PassNC_000015.10Chr1597,274,56297,290,422
essv7000451RemappedPerfectNC_000015.10:g.(?_
97274562)_(9729042
2_?)del
GRCh38.p12First PassNC_000015.10Chr1597,274,56297,290,422
essv7000452RemappedPerfectNC_000015.10:g.(?_
97274562)_(9729042
2_?)del
GRCh38.p12First PassNC_000015.10Chr1597,274,56297,290,422
essv7000453RemappedPerfectNC_000015.10:g.(?_
97274562)_(9729042
2_?)del
GRCh38.p12First PassNC_000015.10Chr1597,274,56297,290,422
essv7000454RemappedPerfectNC_000015.10:g.(?_
97274562)_(9729042
2_?)del
GRCh38.p12First PassNC_000015.10Chr1597,274,56297,290,422
essv7000456RemappedPerfectNC_000015.10:g.(?_
97274562)_(9729042
2_?)del
GRCh38.p12First PassNC_000015.10Chr1597,274,56297,290,422
essv7000457RemappedPerfectNC_000015.10:g.(?_
97274562)_(9729042
2_?)del
GRCh38.p12First PassNC_000015.10Chr1597,274,56297,290,422
essv7000458RemappedPerfectNC_000015.10:g.(?_
97274562)_(9729042
2_?)del
GRCh38.p12First PassNC_000015.10Chr1597,274,56297,290,422
essv7000459RemappedPerfectNC_000015.10:g.(?_
97274562)_(9729042
2_?)del
GRCh38.p12First PassNC_000015.10Chr1597,274,56297,290,422
essv7000460RemappedPerfectNC_000015.10:g.(?_
97274562)_(9729042
2_?)del
GRCh38.p12First PassNC_000015.10Chr1597,274,56297,290,422
essv7000461RemappedPerfectNC_000015.10:g.(?_
97274562)_(9729042
2_?)del
GRCh38.p12First PassNC_000015.10Chr1597,274,56297,290,422
essv7000462RemappedPerfectNC_000015.10:g.(?_
97274562)_(9729042
2_?)del
GRCh38.p12First PassNC_000015.10Chr1597,274,56297,290,422
essv7000463RemappedPerfectNC_000015.10:g.(?_
97274562)_(9729042
2_?)del
GRCh38.p12First PassNC_000015.10Chr1597,274,56297,290,422
essv7000464RemappedPerfectNC_000015.10:g.(?_
97274562)_(9729042
2_?)del
GRCh38.p12First PassNC_000015.10Chr1597,274,56297,290,422
essv7000425RemappedPerfectNC_000015.9:g.(?_9
7808074)_(97833652
_?)del
GRCh37.p13First PassNC_000015.9Chr1597,808,07497,833,652
essv7000426RemappedPerfectNC_000015.9:g.(?_9
7808074)_(97833652
_?)del
GRCh37.p13First PassNC_000015.9Chr1597,808,07497,833,652
essv7000427RemappedPerfectNC_000015.9:g.(?_9
7808074)_(97833652
_?)del
GRCh37.p13First PassNC_000015.9Chr1597,808,07497,833,652
essv7000428RemappedPerfectNC_000015.9:g.(?_9
7817792)_(97828677
_?)del
GRCh37.p13First PassNC_000015.9Chr1597,817,79297,828,677
essv7000429RemappedPerfectNC_000015.9:g.(?_9
7817792)_(97832187
_?)del
GRCh37.p13First PassNC_000015.9Chr1597,817,79297,832,187
essv7000430RemappedPerfectNC_000015.9:g.(?_9
7817792)_(97832187
_?)del
GRCh37.p13First PassNC_000015.9Chr1597,817,79297,832,187
essv7000431RemappedPerfectNC_000015.9:g.(?_9
7817792)_(97832187
_?)del
GRCh37.p13First PassNC_000015.9Chr1597,817,79297,832,187
essv7000432RemappedPerfectNC_000015.9:g.(?_9
7817792)_(97832187
_?)del
GRCh37.p13First PassNC_000015.9Chr1597,817,79297,832,187
essv7000434RemappedPerfectNC_000015.9:g.(?_9
7817792)_(97832187
_?)del
GRCh37.p13First PassNC_000015.9Chr1597,817,79297,832,187
essv7000435RemappedPerfectNC_000015.9:g.(?_9
7817792)_(97832187
_?)del
GRCh37.p13First PassNC_000015.9Chr1597,817,79297,832,187
essv7000436RemappedPerfectNC_000015.9:g.(?_9
7817792)_(97832187
_?)del
GRCh37.p13First PassNC_000015.9Chr1597,817,79297,832,187
essv7000437RemappedPerfectNC_000015.9:g.(?_9
7817792)_(97832187
_?)del
GRCh37.p13First PassNC_000015.9Chr1597,817,79297,832,187
essv7000438RemappedPerfectNC_000015.9:g.(?_9
7817792)_(97832187
_?)del
GRCh37.p13First PassNC_000015.9Chr1597,817,79297,832,187
essv7000439RemappedPerfectNC_000015.9:g.(?_9
7817792)_(97832187
_?)del
GRCh37.p13First PassNC_000015.9Chr1597,817,79297,832,187
essv7000440RemappedPerfectNC_000015.9:g.(?_9
7817792)_(97832187
_?)del
GRCh37.p13First PassNC_000015.9Chr1597,817,79297,832,187
essv7000441RemappedPerfectNC_000015.9:g.(?_9
7817792)_(97832187
_?)del
GRCh37.p13First PassNC_000015.9Chr1597,817,79297,832,187
essv7000442RemappedPerfectNC_000015.9:g.(?_9
7817792)_(97832187
_?)del
GRCh37.p13First PassNC_000015.9Chr1597,817,79297,832,187
essv7000443RemappedPerfectNC_000015.9:g.(?_9
7817792)_(97832187
_?)del
GRCh37.p13First PassNC_000015.9Chr1597,817,79297,832,187
essv7000445RemappedPerfectNC_000015.9:g.(?_9
7817792)_(97832187
_?)del
GRCh37.p13First PassNC_000015.9Chr1597,817,79297,832,187
essv7000446RemappedPerfectNC_000015.9:g.(?_9
7817792)_(97832187
_?)del
GRCh37.p13First PassNC_000015.9Chr1597,817,79297,832,187
essv7000447RemappedPerfectNC_000015.9:g.(?_9
7817792)_(97833652
_?)del
GRCh37.p13First PassNC_000015.9Chr1597,817,79297,833,652
essv7000448RemappedPerfectNC_000015.9:g.(?_9
7817792)_(97833652
_?)del
GRCh37.p13First PassNC_000015.9Chr1597,817,79297,833,652
essv7000449RemappedPerfectNC_000015.9:g.(?_9
7817792)_(97833652
_?)del
GRCh37.p13First PassNC_000015.9Chr1597,817,79297,833,652
essv7000450RemappedPerfectNC_000015.9:g.(?_9
7817792)_(97833652
_?)del
GRCh37.p13First PassNC_000015.9Chr1597,817,79297,833,652
essv7000451RemappedPerfectNC_000015.9:g.(?_9
7817792)_(97833652
_?)del
GRCh37.p13First PassNC_000015.9Chr1597,817,79297,833,652
essv7000452RemappedPerfectNC_000015.9:g.(?_9
7817792)_(97833652
_?)del
GRCh37.p13First PassNC_000015.9Chr1597,817,79297,833,652
essv7000453RemappedPerfectNC_000015.9:g.(?_9
7817792)_(97833652
_?)del
GRCh37.p13First PassNC_000015.9Chr1597,817,79297,833,652
essv7000454RemappedPerfectNC_000015.9:g.(?_9
7817792)_(97833652
_?)del
GRCh37.p13First PassNC_000015.9Chr1597,817,79297,833,652
essv7000456RemappedPerfectNC_000015.9:g.(?_9
7817792)_(97833652
_?)del
GRCh37.p13First PassNC_000015.9Chr1597,817,79297,833,652
essv7000457RemappedPerfectNC_000015.9:g.(?_9
7817792)_(97833652
_?)del
GRCh37.p13First PassNC_000015.9Chr1597,817,79297,833,652
essv7000458RemappedPerfectNC_000015.9:g.(?_9
7817792)_(97833652
_?)del
GRCh37.p13First PassNC_000015.9Chr1597,817,79297,833,652
essv7000459RemappedPerfectNC_000015.9:g.(?_9
7817792)_(97833652
_?)del
GRCh37.p13First PassNC_000015.9Chr1597,817,79297,833,652
essv7000460RemappedPerfectNC_000015.9:g.(?_9
7817792)_(97833652
_?)del
GRCh37.p13First PassNC_000015.9Chr1597,817,79297,833,652
essv7000461RemappedPerfectNC_000015.9:g.(?_9
7817792)_(97833652
_?)del
GRCh37.p13First PassNC_000015.9Chr1597,817,79297,833,652
essv7000462RemappedPerfectNC_000015.9:g.(?_9
7817792)_(97833652
_?)del
GRCh37.p13First PassNC_000015.9Chr1597,817,79297,833,652
essv7000463RemappedPerfectNC_000015.9:g.(?_9
7817792)_(97833652
_?)del
GRCh37.p13First PassNC_000015.9Chr1597,817,79297,833,652
essv7000464RemappedPerfectNC_000015.9:g.(?_9
7817792)_(97833652
_?)del
GRCh37.p13First PassNC_000015.9Chr1597,817,79297,833,652
essv7000425Submitted genomicNC_000015.8:g.(?_9
5609078)_(95634656
_?)del
NCBI36 (hg18)NC_000015.8Chr1595,609,07895,634,656
essv7000426Submitted genomicNC_000015.8:g.(?_9
5609078)_(95634656
_?)del
NCBI36 (hg18)NC_000015.8Chr1595,609,07895,634,656
essv7000427Submitted genomicNC_000015.8:g.(?_9
5609078)_(95634656
_?)del
NCBI36 (hg18)NC_000015.8Chr1595,609,07895,634,656
essv7000428Submitted genomicNC_000015.8:g.(?_9
5618796)_(95629681
_?)del
NCBI36 (hg18)NC_000015.8Chr1595,618,79695,629,681
essv7000429Submitted genomicNC_000015.8:g.(?_9
5618796)_(95633191
_?)del
NCBI36 (hg18)NC_000015.8Chr1595,618,79695,633,191
essv7000430Submitted genomicNC_000015.8:g.(?_9
5618796)_(95633191
_?)del
NCBI36 (hg18)NC_000015.8Chr1595,618,79695,633,191
essv7000431Submitted genomicNC_000015.8:g.(?_9
5618796)_(95633191
_?)del
NCBI36 (hg18)NC_000015.8Chr1595,618,79695,633,191
essv7000432Submitted genomicNC_000015.8:g.(?_9
5618796)_(95633191
_?)del
NCBI36 (hg18)NC_000015.8Chr1595,618,79695,633,191
essv7000434Submitted genomicNC_000015.8:g.(?_9
5618796)_(95633191
_?)del
NCBI36 (hg18)NC_000015.8Chr1595,618,79695,633,191
essv7000435Submitted genomicNC_000015.8:g.(?_9
5618796)_(95633191
_?)del
NCBI36 (hg18)NC_000015.8Chr1595,618,79695,633,191
essv7000436Submitted genomicNC_000015.8:g.(?_9
5618796)_(95633191
_?)del
NCBI36 (hg18)NC_000015.8Chr1595,618,79695,633,191
essv7000437Submitted genomicNC_000015.8:g.(?_9
5618796)_(95633191
_?)del
NCBI36 (hg18)NC_000015.8Chr1595,618,79695,633,191
essv7000438Submitted genomicNC_000015.8:g.(?_9
5618796)_(95633191
_?)del
NCBI36 (hg18)NC_000015.8Chr1595,618,79695,633,191
essv7000439Submitted genomicNC_000015.8:g.(?_9
5618796)_(95633191
_?)del
NCBI36 (hg18)NC_000015.8Chr1595,618,79695,633,191
essv7000440Submitted genomicNC_000015.8:g.(?_9
5618796)_(95633191
_?)del
NCBI36 (hg18)NC_000015.8Chr1595,618,79695,633,191
essv7000441Submitted genomicNC_000015.8:g.(?_9
5618796)_(95633191
_?)del
NCBI36 (hg18)NC_000015.8Chr1595,618,79695,633,191
essv7000442Submitted genomicNC_000015.8:g.(?_9
5618796)_(95633191
_?)del
NCBI36 (hg18)NC_000015.8Chr1595,618,79695,633,191
essv7000443Submitted genomicNC_000015.8:g.(?_9
5618796)_(95633191
_?)del
NCBI36 (hg18)NC_000015.8Chr1595,618,79695,633,191
essv7000445Submitted genomicNC_000015.8:g.(?_9
5618796)_(95633191
_?)del
NCBI36 (hg18)NC_000015.8Chr1595,618,79695,633,191
essv7000446Submitted genomicNC_000015.8:g.(?_9
5618796)_(95633191
_?)del
NCBI36 (hg18)NC_000015.8Chr1595,618,79695,633,191
essv7000447Submitted genomicNC_000015.8:g.(?_9
5618796)_(95634656
_?)del
NCBI36 (hg18)NC_000015.8Chr1595,618,79695,634,656
essv7000448Submitted genomicNC_000015.8:g.(?_9
5618796)_(95634656
_?)del
NCBI36 (hg18)NC_000015.8Chr1595,618,79695,634,656
essv7000449Submitted genomicNC_000015.8:g.(?_9
5618796)_(95634656
_?)del
NCBI36 (hg18)NC_000015.8Chr1595,618,79695,634,656
essv7000450Submitted genomicNC_000015.8:g.(?_9
5618796)_(95634656
_?)del
NCBI36 (hg18)NC_000015.8Chr1595,618,79695,634,656
essv7000451Submitted genomicNC_000015.8:g.(?_9
5618796)_(95634656
_?)del
NCBI36 (hg18)NC_000015.8Chr1595,618,79695,634,656
essv7000452Submitted genomicNC_000015.8:g.(?_9
5618796)_(95634656
_?)del
NCBI36 (hg18)NC_000015.8Chr1595,618,79695,634,656
Showing 100 of 111

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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