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nsv5973955

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:35,582

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 441 SVs from 34 studies. See in: genome view    
Submitted genomic56,099,508-56,135,089Question Mark
Overlapping variant regions from other studies: 440 SVs from 34 studies. See in: genome view    
Remapped(Score: Perfect):56,125,941-56,161,522Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5973955Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX56,099,50856,135,089
nsv5973955RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX56,125,94156,161,522

Variant Call Information

Variant Call IDTypeMethodAnalysisCopy number
nssv17516394copy number variationSequencingSequence alignment2

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv17516394Submitted genomicGRCh38 (hg38)NC_000023.11ChrX56,099,50856,135,089
nssv17516394RemappedPerfectGRCh37.p13First PassNC_000023.10ChrX56,125,94156,161,522

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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