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nsv4042360

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:536,376

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 915 SVs from 17 studies. See in: genome view    
Remapped(Score: Pass):1,907,463-2,443,838Question Mark
Overlapping variant regions from other studies: 806 SVs from 17 studies. See in: genome view    
Submitted genomic2,026,356-2,361,879Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4042360RemappedPassGRCh38.p12Primary AssemblyFirst PassNC_000023.11ChrX1,907,4632,443,838
nsv4042360Submitted genomicGRCh37.p13Primary AssemblyNC_000023.10ChrX2,026,3562,361,879

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15988085duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15988085RemappedPassNC_000023.11:g.190
7463_2443838dup
GRCh38.p12First PassNC_000023.11ChrX1,907,4632,443,838
nssv15988085Submitted genomicNC_000023.10:g.202
6356_2361879dup
GRCh37.p13NC_000023.10ChrX2,026,3562,361,879

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)
nssv159880854.6e-005121640
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