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nsv3170234

  • Variant Calls:13
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,900

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 371 SVs from 64 studies. See in: genome view    
Remapped(Score: Perfect):28,044,706-28,055,605Question Mark
Overlapping variant regions from other studies: 377 SVs from 65 studies. See in: genome view    
Remapped(Score: Perfect):28,044,704-28,055,603Question Mark
Overlapping variant regions from other studies: 152 SVs from 24 studies. See in: genome view    
Submitted genomic28,034,704-28,045,603Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv3170234RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr928,044,70628,047,59028,050,69328,055,605
nsv3170234RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr928,044,70428,047,58828,050,69128,055,603
nsv3170234Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000009.10Chr928,034,70428,037,58828,040,69128,045,603

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisCopy numberOther Calls in this Sample and Study
nssv14243538deletionSNI_7SNP arraySNP genotyping analysis1128
nssv14243564deletionNGO_35SNP arraySNP genotyping analysis1111
nssv14244329deletionMLY_6SNP arraySNP genotyping analysis1132
nssv14244611deletionNGO_22SNP arraySNP genotyping analysis1126
nssv14245082deletionSNI_9SNP arraySNP genotyping analysis0128
nssv14247243deletionNGO_23SNP arraySNP genotyping analysis1127
nssv14247934deletionNGO_31SNP arraySNP genotyping analysis0121
nssv14249699deletionNGO_12SNP arraySNP genotyping analysis1117
nssv14250199deletionNGO_52SNP arraySNP genotyping analysis1123
nssv14250518deletionSNI_11SNP arraySNP genotyping analysis1129
nssv14250893deletionNGO_11SNP arraySNP genotyping analysis1131
nssv14251970deletionSNI_14SNP arraySNP genotyping analysis1136
nssv14252482duplicationNGO_6SNP arraySNP genotyping analysis3141

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv14243538RemappedPerfectNC_000009.12:g.(28
044706_28047590)_(
28050693_28055605)
del
GRCh38.p12First PassNC_000009.12Chr928,044,70628,047,59028,050,69328,055,605
nssv14243564RemappedPerfectNC_000009.12:g.(28
044706_28047590)_(
28050693_28055605)
del
GRCh38.p12First PassNC_000009.12Chr928,044,70628,047,59028,050,69328,055,605
nssv14244329RemappedPerfectNC_000009.12:g.(28
044706_28047590)_(
28050693_28055605)
del
GRCh38.p12First PassNC_000009.12Chr928,044,70628,047,59028,050,69328,055,605
nssv14244611RemappedPerfectNC_000009.12:g.(28
044706_28047590)_(
28050693_28055605)
del
GRCh38.p12First PassNC_000009.12Chr928,044,70628,047,59028,050,69328,055,605
nssv14245082RemappedPerfectNC_000009.12:g.(28
044706_28047590)_(
28050693_28055605)
del
GRCh38.p12First PassNC_000009.12Chr928,044,70628,047,59028,050,69328,055,605
nssv14247243RemappedPerfectNC_000009.12:g.(28
044706_28047590)_(
28050693_28055605)
del
GRCh38.p12First PassNC_000009.12Chr928,044,70628,047,59028,050,69328,055,605
nssv14247934RemappedPerfectNC_000009.12:g.(28
044706_28047590)_(
28050693_28055605)
del
GRCh38.p12First PassNC_000009.12Chr928,044,70628,047,59028,050,69328,055,605
nssv14249699RemappedPerfectNC_000009.12:g.(28
044706_28047590)_(
28050693_28055605)
del
GRCh38.p12First PassNC_000009.12Chr928,044,70628,047,59028,050,69328,055,605
nssv14250199RemappedPerfectNC_000009.12:g.(28
044706_28047590)_(
28050693_28055605)
del
GRCh38.p12First PassNC_000009.12Chr928,044,70628,047,59028,050,69328,055,605
nssv14250518RemappedPerfectNC_000009.12:g.(28
044706_28047590)_(
28050693_28055605)
del
GRCh38.p12First PassNC_000009.12Chr928,044,70628,047,59028,050,69328,055,605
nssv14250893RemappedPerfectNC_000009.12:g.(28
044706_28047590)_(
28050693_28055605)
del
GRCh38.p12First PassNC_000009.12Chr928,044,70628,047,59028,050,69328,055,605
nssv14251970RemappedPerfectNC_000009.12:g.(28
044706_28047590)_(
28050693_28055605)
del
GRCh38.p12First PassNC_000009.12Chr928,044,70628,047,59028,050,69328,055,605
nssv14252482RemappedPerfectNC_000009.12:g.(28
044706_28047590)_(
28050693_28055605)
dup
GRCh38.p12First PassNC_000009.12Chr928,044,70628,047,59028,050,69328,055,605
nssv14243538RemappedPerfectNC_000009.11:g.(28
044704_28047588)_(
28050691_28055603)
del
GRCh37.p13First PassNC_000009.11Chr928,044,70428,047,58828,050,69128,055,603
nssv14243564RemappedPerfectNC_000009.11:g.(28
044704_28047588)_(
28050691_28055603)
del
GRCh37.p13First PassNC_000009.11Chr928,044,70428,047,58828,050,69128,055,603
nssv14244329RemappedPerfectNC_000009.11:g.(28
044704_28047588)_(
28050691_28055603)
del
GRCh37.p13First PassNC_000009.11Chr928,044,70428,047,58828,050,69128,055,603
nssv14244611RemappedPerfectNC_000009.11:g.(28
044704_28047588)_(
28050691_28055603)
del
GRCh37.p13First PassNC_000009.11Chr928,044,70428,047,58828,050,69128,055,603
nssv14245082RemappedPerfectNC_000009.11:g.(28
044704_28047588)_(
28050691_28055603)
del
GRCh37.p13First PassNC_000009.11Chr928,044,70428,047,58828,050,69128,055,603
nssv14247243RemappedPerfectNC_000009.11:g.(28
044704_28047588)_(
28050691_28055603)
del
GRCh37.p13First PassNC_000009.11Chr928,044,70428,047,58828,050,69128,055,603
nssv14247934RemappedPerfectNC_000009.11:g.(28
044704_28047588)_(
28050691_28055603)
del
GRCh37.p13First PassNC_000009.11Chr928,044,70428,047,58828,050,69128,055,603
nssv14249699RemappedPerfectNC_000009.11:g.(28
044704_28047588)_(
28050691_28055603)
del
GRCh37.p13First PassNC_000009.11Chr928,044,70428,047,58828,050,69128,055,603
nssv14250199RemappedPerfectNC_000009.11:g.(28
044704_28047588)_(
28050691_28055603)
del
GRCh37.p13First PassNC_000009.11Chr928,044,70428,047,58828,050,69128,055,603
nssv14250518RemappedPerfectNC_000009.11:g.(28
044704_28047588)_(
28050691_28055603)
del
GRCh37.p13First PassNC_000009.11Chr928,044,70428,047,58828,050,69128,055,603
nssv14250893RemappedPerfectNC_000009.11:g.(28
044704_28047588)_(
28050691_28055603)
del
GRCh37.p13First PassNC_000009.11Chr928,044,70428,047,58828,050,69128,055,603
nssv14251970RemappedPerfectNC_000009.11:g.(28
044704_28047588)_(
28050691_28055603)
del
GRCh37.p13First PassNC_000009.11Chr928,044,70428,047,58828,050,69128,055,603
nssv14252482RemappedPerfectNC_000009.11:g.(28
044704_28047588)_(
28050691_28055603)
dup
GRCh37.p13First PassNC_000009.11Chr928,044,70428,047,58828,050,69128,055,603
nssv14243538Submitted genomicNC_000009.10:g.(28
034704_28037588)_(
28040691_28045603)
del
NCBI36 (hg18)NC_000009.10Chr928,034,70428,037,58828,040,69128,045,603
nssv14243564Submitted genomicNC_000009.10:g.(28
034704_28037588)_(
28040691_28045603)
del
NCBI36 (hg18)NC_000009.10Chr928,034,70428,037,58828,040,69128,045,603
nssv14244329Submitted genomicNC_000009.10:g.(28
034704_28037588)_(
28040691_28045603)
del
NCBI36 (hg18)NC_000009.10Chr928,034,70428,037,58828,040,69128,045,603
nssv14244611Submitted genomicNC_000009.10:g.(28
034704_28037588)_(
28040691_28045603)
del
NCBI36 (hg18)NC_000009.10Chr928,034,70428,037,58828,040,69128,045,603
nssv14245082Submitted genomicNC_000009.10:g.(28
034704_28037588)_(
28040691_28045603)
del
NCBI36 (hg18)NC_000009.10Chr928,034,70428,037,58828,040,69128,045,603
nssv14247243Submitted genomicNC_000009.10:g.(28
034704_28037588)_(
28040691_28045603)
del
NCBI36 (hg18)NC_000009.10Chr928,034,70428,037,58828,040,69128,045,603
nssv14247934Submitted genomicNC_000009.10:g.(28
034704_28037588)_(
28040691_28045603)
del
NCBI36 (hg18)NC_000009.10Chr928,034,70428,037,58828,040,69128,045,603
nssv14249699Submitted genomicNC_000009.10:g.(28
034704_28037588)_(
28040691_28045603)
del
NCBI36 (hg18)NC_000009.10Chr928,034,70428,037,58828,040,69128,045,603
nssv14250199Submitted genomicNC_000009.10:g.(28
034704_28037588)_(
28040691_28045603)
del
NCBI36 (hg18)NC_000009.10Chr928,034,70428,037,58828,040,69128,045,603
nssv14250518Submitted genomicNC_000009.10:g.(28
034704_28037588)_(
28040691_28045603)
del
NCBI36 (hg18)NC_000009.10Chr928,034,70428,037,58828,040,69128,045,603
nssv14250893Submitted genomicNC_000009.10:g.(28
034704_28037588)_(
28040691_28045603)
del
NCBI36 (hg18)NC_000009.10Chr928,034,70428,037,58828,040,69128,045,603
nssv14251970Submitted genomicNC_000009.10:g.(28
034704_28037588)_(
28040691_28045603)
del
NCBI36 (hg18)NC_000009.10Chr928,034,70428,037,58828,040,69128,045,603
nssv14252482Submitted genomicNC_000009.10:g.(28
034704_28037588)_(
28040691_28045603)
dup
NCBI36 (hg18)NC_000009.10Chr928,034,70428,037,58828,040,69128,045,603

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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