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nsv6629664

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:156,767

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1562 SVs from 89 studies. See in: genome view    
Remapped(Score: Perfect):189,837,729-189,994,495Question Mark
Overlapping variant regions from other studies: 1518 SVs from 88 studies. See in: genome view    
Submitted genomic190,758,884-190,915,650Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv6629664RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000004.12Chr4189,837,729189,994,495
nsv6629664Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000004.11Chr4190,758,884190,915,650

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv18285721duplicationOSC2822SNP arrayProbe signal intensity5

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv18285721RemappedPerfectNC_000004.12:g.(?_
189837729)_(189994
495_?)dup
GRCh38.p12First PassNC_000004.12Chr4189,837,729189,994,495
nssv18285721Submitted genomicNC_000004.11:g.(?_
190758884)_(190915
650_?)dup
GRCh37 (hg19)NC_000004.11Chr4190,758,884190,915,650

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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