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nsv4380296

  • Variant Calls:3
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:155,752,212

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 236290 SVs from 124 studies. See in: genome view    
Remapped(Score: Good):251,880-156,004,091Question Mark
Overlapping variant regions from other studies: 235448 SVs from 124 studies. See in: genome view    
Submitted genomic168,547-155,233,756Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv4380296RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000023.11ChrX251,880156,004,091
nsv4380296Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000023.10ChrX168,547155,233,756

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv15644333copy number variation16-1006-001SNP arrayGenotyping24
nssv15666924copy number variation7-0142-003SNP arrayGenotyping23
nssv15675000copy number variation208032SNP arrayGenotyping19

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv15644333RemappedGoodGRCh38.p12First PassNC_000023.11ChrX251,880156,004,091
nssv15666924RemappedGoodGRCh38.p12First PassNC_000023.11ChrX251,880156,004,091
nssv15675000RemappedGoodGRCh38.p12First PassNC_000023.11ChrX251,880156,004,091
nssv15644333Submitted genomicGRCh37 (hg19)NC_000023.10ChrX168,547155,233,756
nssv15666924Submitted genomicGRCh37 (hg19)NC_000023.10ChrX168,547155,233,756
nssv15675000Submitted genomicGRCh37 (hg19)NC_000023.10ChrX168,547155,233,756

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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