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esv2760907

  • Variant Calls:25
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,918

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 374 SVs from 55 studies. See in: genome view    
Remapped(Score: Perfect):180,209,255-180,217,172Question Mark
Overlapping variant regions from other studies: 374 SVs from 55 studies. See in: genome view    
Remapped(Score: Perfect):181,130,408-181,138,325Question Mark
Overlapping variant regions from other studies: 204 SVs from 21 studies. See in: genome view    
Submitted genomic181,367,402-181,375,319Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartOuter Stop
esv2760907RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000004.12Chr4180,209,255180,217,172
esv2760907RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4181,130,408181,138,325
esv2760907Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000004.10Chr4181,367,402181,375,319

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv7012318copy number lossRW_0604SNP arraySNP genotyping analysis43
essv7012319copy number lossRW_0003SNP arraySNP genotyping analysis58
essv7012320copy number lossRW_0020SNP arraySNP genotyping analysis76
essv7012321copy number lossRW_0023SNP arraySNP genotyping analysis71
essv7012323copy number lossRW_0039SNP arraySNP genotyping analysis56
essv7012324copy number lossRW_0058SNP arraySNP genotyping analysis45
essv7012325copy number lossRW_0088SNP arraySNP genotyping analysis51
essv7012326copy number lossRW_0115SNP arraySNP genotyping analysis50
essv7012327copy number lossRW_0116SNP arraySNP genotyping analysis59
essv7012328copy number lossRW_0171SNP arraySNP genotyping analysis65
essv7012329copy number lossRW_0176SNP arraySNP genotyping analysis58
essv7012330copy number lossRW_0184SNP arraySNP genotyping analysis47
essv7012331copy number lossRW_0215SNP arraySNP genotyping analysis69
essv7012332copy number lossRW_0221SNP arraySNP genotyping analysis69
essv7012334copy number lossRW_0226SNP arraySNP genotyping analysis58
essv7012335copy number lossRW_0237SNP arraySNP genotyping analysis55
essv7012336copy number lossRW_0250SNP arraySNP genotyping analysis65
essv7012337copy number lossRW_0257SNP arraySNP genotyping analysis61
essv7012338copy number lossRW_0281SNP arraySNP genotyping analysis58
essv7012339copy number lossRW_0309SNP arraySNP genotyping analysis43
essv7012340copy number lossRW_0358SNP arraySNP genotyping analysis42
essv7012341copy number lossRW_0521SNP arraySNP genotyping analysis39
essv7012342copy number lossRW_0605SNP arraySNP genotyping analysis56
essv7012343copy number lossRW_0620SNP arraySNP genotyping analysis39
essv7012345copy number lossRW_0625SNP arraySNP genotyping analysis50

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv7012318RemappedPerfectNC_000004.12:g.(?_
180209255)_(180217
172_?)del
GRCh38.p12First PassNC_000004.12Chr4180,209,255180,217,172
essv7012319RemappedPerfectNC_000004.12:g.(?_
180215918)_(180217
172_?)del
GRCh38.p12First PassNC_000004.12Chr4180,215,918180,217,172
essv7012320RemappedPerfectNC_000004.12:g.(?_
180215918)_(180217
172_?)del
GRCh38.p12First PassNC_000004.12Chr4180,215,918180,217,172
essv7012321RemappedPerfectNC_000004.12:g.(?_
180215918)_(180217
172_?)del
GRCh38.p12First PassNC_000004.12Chr4180,215,918180,217,172
essv7012323RemappedPerfectNC_000004.12:g.(?_
180215918)_(180217
172_?)del
GRCh38.p12First PassNC_000004.12Chr4180,215,918180,217,172
essv7012324RemappedPerfectNC_000004.12:g.(?_
180215918)_(180217
172_?)del
GRCh38.p12First PassNC_000004.12Chr4180,215,918180,217,172
essv7012325RemappedPerfectNC_000004.12:g.(?_
180215918)_(180217
172_?)del
GRCh38.p12First PassNC_000004.12Chr4180,215,918180,217,172
essv7012326RemappedPerfectNC_000004.12:g.(?_
180215918)_(180217
172_?)del
GRCh38.p12First PassNC_000004.12Chr4180,215,918180,217,172
essv7012327RemappedPerfectNC_000004.12:g.(?_
180215918)_(180217
172_?)del
GRCh38.p12First PassNC_000004.12Chr4180,215,918180,217,172
essv7012328RemappedPerfectNC_000004.12:g.(?_
180215918)_(180217
172_?)del
GRCh38.p12First PassNC_000004.12Chr4180,215,918180,217,172
essv7012329RemappedPerfectNC_000004.12:g.(?_
180215918)_(180217
172_?)del
GRCh38.p12First PassNC_000004.12Chr4180,215,918180,217,172
essv7012330RemappedPerfectNC_000004.12:g.(?_
180215918)_(180217
172_?)del
GRCh38.p12First PassNC_000004.12Chr4180,215,918180,217,172
essv7012331RemappedPerfectNC_000004.12:g.(?_
180215918)_(180217
172_?)del
GRCh38.p12First PassNC_000004.12Chr4180,215,918180,217,172
essv7012332RemappedPerfectNC_000004.12:g.(?_
180215918)_(180217
172_?)del
GRCh38.p12First PassNC_000004.12Chr4180,215,918180,217,172
essv7012334RemappedPerfectNC_000004.12:g.(?_
180215918)_(180217
172_?)del
GRCh38.p12First PassNC_000004.12Chr4180,215,918180,217,172
essv7012335RemappedPerfectNC_000004.12:g.(?_
180215918)_(180217
172_?)del
GRCh38.p12First PassNC_000004.12Chr4180,215,918180,217,172
essv7012336RemappedPerfectNC_000004.12:g.(?_
180215918)_(180217
172_?)del
GRCh38.p12First PassNC_000004.12Chr4180,215,918180,217,172
essv7012337RemappedPerfectNC_000004.12:g.(?_
180215918)_(180217
172_?)del
GRCh38.p12First PassNC_000004.12Chr4180,215,918180,217,172
essv7012338RemappedPerfectNC_000004.12:g.(?_
180215918)_(180217
172_?)del
GRCh38.p12First PassNC_000004.12Chr4180,215,918180,217,172
essv7012339RemappedPerfectNC_000004.12:g.(?_
180215918)_(180217
172_?)del
GRCh38.p12First PassNC_000004.12Chr4180,215,918180,217,172
essv7012340RemappedPerfectNC_000004.12:g.(?_
180215918)_(180217
172_?)del
GRCh38.p12First PassNC_000004.12Chr4180,215,918180,217,172
essv7012341RemappedPerfectNC_000004.12:g.(?_
180215918)_(180217
172_?)del
GRCh38.p12First PassNC_000004.12Chr4180,215,918180,217,172
essv7012342RemappedPerfectNC_000004.12:g.(?_
180215918)_(180217
172_?)del
GRCh38.p12First PassNC_000004.12Chr4180,215,918180,217,172
essv7012343RemappedPerfectNC_000004.12:g.(?_
180215918)_(180217
172_?)del
GRCh38.p12First PassNC_000004.12Chr4180,215,918180,217,172
essv7012345RemappedPerfectNC_000004.12:g.(?_
180215918)_(180217
172_?)del
GRCh38.p12First PassNC_000004.12Chr4180,215,918180,217,172
essv7012318RemappedPerfectNC_000004.11:g.(?_
181130408)_(181138
325_?)del
GRCh37.p13First PassNC_000004.11Chr4181,130,408181,138,325
essv7012319RemappedPerfectNC_000004.11:g.(?_
181137071)_(181138
325_?)del
GRCh37.p13First PassNC_000004.11Chr4181,137,071181,138,325
essv7012320RemappedPerfectNC_000004.11:g.(?_
181137071)_(181138
325_?)del
GRCh37.p13First PassNC_000004.11Chr4181,137,071181,138,325
essv7012321RemappedPerfectNC_000004.11:g.(?_
181137071)_(181138
325_?)del
GRCh37.p13First PassNC_000004.11Chr4181,137,071181,138,325
essv7012323RemappedPerfectNC_000004.11:g.(?_
181137071)_(181138
325_?)del
GRCh37.p13First PassNC_000004.11Chr4181,137,071181,138,325
essv7012324RemappedPerfectNC_000004.11:g.(?_
181137071)_(181138
325_?)del
GRCh37.p13First PassNC_000004.11Chr4181,137,071181,138,325
essv7012325RemappedPerfectNC_000004.11:g.(?_
181137071)_(181138
325_?)del
GRCh37.p13First PassNC_000004.11Chr4181,137,071181,138,325
essv7012326RemappedPerfectNC_000004.11:g.(?_
181137071)_(181138
325_?)del
GRCh37.p13First PassNC_000004.11Chr4181,137,071181,138,325
essv7012327RemappedPerfectNC_000004.11:g.(?_
181137071)_(181138
325_?)del
GRCh37.p13First PassNC_000004.11Chr4181,137,071181,138,325
essv7012328RemappedPerfectNC_000004.11:g.(?_
181137071)_(181138
325_?)del
GRCh37.p13First PassNC_000004.11Chr4181,137,071181,138,325
essv7012329RemappedPerfectNC_000004.11:g.(?_
181137071)_(181138
325_?)del
GRCh37.p13First PassNC_000004.11Chr4181,137,071181,138,325
essv7012330RemappedPerfectNC_000004.11:g.(?_
181137071)_(181138
325_?)del
GRCh37.p13First PassNC_000004.11Chr4181,137,071181,138,325
essv7012331RemappedPerfectNC_000004.11:g.(?_
181137071)_(181138
325_?)del
GRCh37.p13First PassNC_000004.11Chr4181,137,071181,138,325
essv7012332RemappedPerfectNC_000004.11:g.(?_
181137071)_(181138
325_?)del
GRCh37.p13First PassNC_000004.11Chr4181,137,071181,138,325
essv7012334RemappedPerfectNC_000004.11:g.(?_
181137071)_(181138
325_?)del
GRCh37.p13First PassNC_000004.11Chr4181,137,071181,138,325
essv7012335RemappedPerfectNC_000004.11:g.(?_
181137071)_(181138
325_?)del
GRCh37.p13First PassNC_000004.11Chr4181,137,071181,138,325
essv7012336RemappedPerfectNC_000004.11:g.(?_
181137071)_(181138
325_?)del
GRCh37.p13First PassNC_000004.11Chr4181,137,071181,138,325
essv7012337RemappedPerfectNC_000004.11:g.(?_
181137071)_(181138
325_?)del
GRCh37.p13First PassNC_000004.11Chr4181,137,071181,138,325
essv7012338RemappedPerfectNC_000004.11:g.(?_
181137071)_(181138
325_?)del
GRCh37.p13First PassNC_000004.11Chr4181,137,071181,138,325
essv7012339RemappedPerfectNC_000004.11:g.(?_
181137071)_(181138
325_?)del
GRCh37.p13First PassNC_000004.11Chr4181,137,071181,138,325
essv7012340RemappedPerfectNC_000004.11:g.(?_
181137071)_(181138
325_?)del
GRCh37.p13First PassNC_000004.11Chr4181,137,071181,138,325
essv7012341RemappedPerfectNC_000004.11:g.(?_
181137071)_(181138
325_?)del
GRCh37.p13First PassNC_000004.11Chr4181,137,071181,138,325
essv7012342RemappedPerfectNC_000004.11:g.(?_
181137071)_(181138
325_?)del
GRCh37.p13First PassNC_000004.11Chr4181,137,071181,138,325
essv7012343RemappedPerfectNC_000004.11:g.(?_
181137071)_(181138
325_?)del
GRCh37.p13First PassNC_000004.11Chr4181,137,071181,138,325
essv7012345RemappedPerfectNC_000004.11:g.(?_
181137071)_(181138
325_?)del
GRCh37.p13First PassNC_000004.11Chr4181,137,071181,138,325
essv7012318Submitted genomicNC_000004.10:g.(?_
181367402)_(181375
319_?)del
NCBI36 (hg18)NC_000004.10Chr4181,367,402181,375,319
essv7012319Submitted genomicNC_000004.10:g.(?_
181374065)_(181375
319_?)del
NCBI36 (hg18)NC_000004.10Chr4181,374,065181,375,319
essv7012320Submitted genomicNC_000004.10:g.(?_
181374065)_(181375
319_?)del
NCBI36 (hg18)NC_000004.10Chr4181,374,065181,375,319
essv7012321Submitted genomicNC_000004.10:g.(?_
181374065)_(181375
319_?)del
NCBI36 (hg18)NC_000004.10Chr4181,374,065181,375,319
essv7012323Submitted genomicNC_000004.10:g.(?_
181374065)_(181375
319_?)del
NCBI36 (hg18)NC_000004.10Chr4181,374,065181,375,319
essv7012324Submitted genomicNC_000004.10:g.(?_
181374065)_(181375
319_?)del
NCBI36 (hg18)NC_000004.10Chr4181,374,065181,375,319
essv7012325Submitted genomicNC_000004.10:g.(?_
181374065)_(181375
319_?)del
NCBI36 (hg18)NC_000004.10Chr4181,374,065181,375,319
essv7012326Submitted genomicNC_000004.10:g.(?_
181374065)_(181375
319_?)del
NCBI36 (hg18)NC_000004.10Chr4181,374,065181,375,319
essv7012327Submitted genomicNC_000004.10:g.(?_
181374065)_(181375
319_?)del
NCBI36 (hg18)NC_000004.10Chr4181,374,065181,375,319
essv7012328Submitted genomicNC_000004.10:g.(?_
181374065)_(181375
319_?)del
NCBI36 (hg18)NC_000004.10Chr4181,374,065181,375,319
essv7012329Submitted genomicNC_000004.10:g.(?_
181374065)_(181375
319_?)del
NCBI36 (hg18)NC_000004.10Chr4181,374,065181,375,319
essv7012330Submitted genomicNC_000004.10:g.(?_
181374065)_(181375
319_?)del
NCBI36 (hg18)NC_000004.10Chr4181,374,065181,375,319
essv7012331Submitted genomicNC_000004.10:g.(?_
181374065)_(181375
319_?)del
NCBI36 (hg18)NC_000004.10Chr4181,374,065181,375,319
essv7012332Submitted genomicNC_000004.10:g.(?_
181374065)_(181375
319_?)del
NCBI36 (hg18)NC_000004.10Chr4181,374,065181,375,319
essv7012334Submitted genomicNC_000004.10:g.(?_
181374065)_(181375
319_?)del
NCBI36 (hg18)NC_000004.10Chr4181,374,065181,375,319
essv7012335Submitted genomicNC_000004.10:g.(?_
181374065)_(181375
319_?)del
NCBI36 (hg18)NC_000004.10Chr4181,374,065181,375,319
essv7012336Submitted genomicNC_000004.10:g.(?_
181374065)_(181375
319_?)del
NCBI36 (hg18)NC_000004.10Chr4181,374,065181,375,319
essv7012337Submitted genomicNC_000004.10:g.(?_
181374065)_(181375
319_?)del
NCBI36 (hg18)NC_000004.10Chr4181,374,065181,375,319
essv7012338Submitted genomicNC_000004.10:g.(?_
181374065)_(181375
319_?)del
NCBI36 (hg18)NC_000004.10Chr4181,374,065181,375,319
essv7012339Submitted genomicNC_000004.10:g.(?_
181374065)_(181375
319_?)del
NCBI36 (hg18)NC_000004.10Chr4181,374,065181,375,319
essv7012340Submitted genomicNC_000004.10:g.(?_
181374065)_(181375
319_?)del
NCBI36 (hg18)NC_000004.10Chr4181,374,065181,375,319
essv7012341Submitted genomicNC_000004.10:g.(?_
181374065)_(181375
319_?)del
NCBI36 (hg18)NC_000004.10Chr4181,374,065181,375,319
essv7012342Submitted genomicNC_000004.10:g.(?_
181374065)_(181375
319_?)del
NCBI36 (hg18)NC_000004.10Chr4181,374,065181,375,319
essv7012343Submitted genomicNC_000004.10:g.(?_
181374065)_(181375
319_?)del
NCBI36 (hg18)NC_000004.10Chr4181,374,065181,375,319
essv7012345Submitted genomicNC_000004.10:g.(?_
181374065)_(181375
319_?)del
NCBI36 (hg18)NC_000004.10Chr4181,374,065181,375,319

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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