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nsv5424625

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,372

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 270 SVs from 34 studies. See in: genome view    
Submitted genomic68,325,585-68,327,956Question Mark
Overlapping variant regions from other studies: 270 SVs from 34 studies. See in: genome view    
Remapped(Score: Perfect):67,545,427-67,547,798Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5424625Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX68,325,58568,327,956
nsv5424625RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX67,545,42767,547,798

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17740521deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17740521Submitted genomicNC_000023.11:g.683
25585_68327956del
GRCh38 (hg38)NC_000023.11ChrX68,325,58568,327,956
nssv17740521RemappedPerfectNC_000023.10:g.675
45427_67547798del
GRCh37.p13First PassNC_000023.10ChrX67,545,42767,547,798

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv177405210.0684336404
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