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nsv949742

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,012,024

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2483 SVs from 77 studies. See in: genome view    
Remapped(Score: Perfect):6,903,064-7,915,087Question Mark
Overlapping variant regions from other studies: 2494 SVs from 79 studies. See in: genome view    
Remapped(Score: Good):6,821,105-7,883,128Question Mark
Overlapping variant regions from other studies: 160 SVs from 10 studies. See in: genome view    
Submitted genomic6,680,841-7,692,864Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv949742RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000023.11ChrX6,903,0647,915,087
nsv949742RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX6,821,1057,883,128
nsv949742Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000023.8ChrX6,680,8417,692,864

Variant Call Information

Variant Call IDTypeMethodAnalysisCopy number
nssv2768495copy number lossSNP arraySNP genotyping analysis1

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv2768495RemappedPerfectNC_000023.11:g.(?_
6903064)_(7915087_
?)del
GRCh38.p12First PassNC_000023.11ChrX6,903,0647,915,087
nssv2768495RemappedGoodNC_000023.10:g.(?_
6821105)_(7883128_
?)del
GRCh37.p13First PassNC_000023.10ChrX6,821,1057,883,128
nssv2768495Submitted genomicNC_000023.8:g.(?_6
680841)_(7692864_?
)del
NCBI35 (hg17)NC_000023.8ChrX6,680,8417,692,864

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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