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nsv949751

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:323,086

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 3472 SVs from 59 studies. See in: genome view    
Remapped(Score: Perfect):1,212,757-1,535,842Question Mark
Overlapping variant regions from other studies: 3473 SVs from 59 studies. See in: genome view    
Submitted genomic1,331,650-1,654,735Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv949751RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000023.11ChrX1,212,7571,535,842
nsv949751Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000023.10ChrX1,331,6501,654,735

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysis
nssv2995880deletion961SequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv2995880RemappedPerfectNC_000023.11:g.121
2757_1535842del
GRCh38.p12First PassNC_000023.11ChrX1,212,7571,535,842
nssv2995880Submitted genomicNC_000023.10:g.133
1650_1654735del
GRCh37 (hg19)NC_000023.10ChrX1,331,6501,654,735

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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