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nsv4369708

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:167,146

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 911 SVs from 87 studies. See in: genome view    
Remapped(Score: Pass):142,618,685-142,785,830Question Mark
Overlapping variant regions from other studies: 1081 SVs from 77 studies. See in: genome view    
Remapped(Score: Pass):656,734-781,128Question Mark
Overlapping variant regions from other studies: 1517 SVs from 102 studies. See in: genome view    
Submitted genomic142,246,905-142,493,639Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv4369708RemappedPassGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7142,618,685142,785,830
nsv4369708RemappedPassGRCh38.p12ALT_REF_LOCI_1First PassNT_187562.1Chr7|NT_18
7562.1
656,734781,128
nsv4369708Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr7142,246,905142,493,639

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv15680703copy number gain215271SNP arrayGenotyping21

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv15680703RemappedPassNT_187562.1:g.(?_6
56734)_(781128_?)d
up
GRCh38.p12First PassNT_187562.1Chr7|NT_18
7562.1
656,734781,128
nssv15680703RemappedPassNC_000007.14:g.(?_
142618685)_(142785
830_?)dup
GRCh38.p12First PassNC_000007.14Chr7142,618,685142,785,830
nssv15680703Submitted genomicNC_000007.13:g.(?_
142246905)_(142493
639_?)dup
GRCh37 (hg19)NC_000007.13Chr7142,246,905142,493,639

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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