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nsv6631800

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:86,507

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 366 SVs from 55 studies. See in: genome view    
Remapped(Score: Good):101,539,827-101,626,333Question Mark
Overlapping variant regions from other studies: 366 SVs from 55 studies. See in: genome view    
Submitted genomic101,183,108-101,269,613Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv6631800RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7101,539,827101,626,333
nsv6631800Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr7101,183,108101,269,613

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv18312951duplicationOSC7685SNP arrayProbe signal intensity12

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv18312951RemappedGoodNC_000007.14:g.(?_
101539827)_(101626
333_?)dup
GRCh38.p12First PassNC_000007.14Chr7101,539,827101,626,333
nssv18312951Submitted genomicNC_000007.13:g.(?_
101183108)_(101269
613_?)dup
GRCh37 (hg19)NC_000007.13Chr7101,183,108101,269,613

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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