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nsv5554044

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 250 SVs from 19 studies. See in: genome view    
Submitted genomic138,915,848-138,915,899Question Mark
Overlapping variant regions from other studies: 250 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):137,998,010-137,998,061Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5554044Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX138,915,848138,915,899
nsv5554044RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX137,998,010137,998,061

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17742622sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17742622Submitted genomicNC_000023.11:g.138
915848_138915899in
s717
GRCh38 (hg38)NC_000023.11ChrX138,915,848138,915,899
nssv17742622RemappedPerfectNC_000023.10:g.137
998010_137998061in
s717
GRCh37.p13First PassNC_000023.10ChrX137,998,010137,998,061

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)
nssv17742622<0.00116404
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