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nsv4042743

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:177,301

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 180 SVs from 5 studies. See in: genome view    
Remapped(Score: Perfect):22,879,803-23,057,103Question Mark
Overlapping variant regions from other studies: 181 SVs from 5 studies. See in: genome view    
Submitted genomic25,025,950-25,203,250Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4042743RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000024.10ChrY22,879,80323,057,103
nsv4042743Submitted genomicGRCh37.p13Primary AssemblyNC_000024.9ChrY25,025,95025,203,250

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15991013duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15991013RemappedPerfectNC_000024.10:g.228
79803_23057103dup
GRCh38.p12First PassNC_000024.10ChrY22,879,80323,057,103
nssv15991013Submitted genomicNC_000024.9:g.2502
5950_25203250dup
GRCh37.p13NC_000024.9ChrY25,025,95025,203,250

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)
nssv159910130.01212910978
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