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nsv5545368

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 260 SVs from 23 studies. See in: genome view    
Submitted genomic110,741,228-110,741,228Question Mark
Overlapping variant regions from other studies: 260 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):109,984,456-109,984,456Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5545368Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX110,741,228110,741,228
nsv5545368RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX109,984,456109,984,456

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17741968insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17741968Submitted genomicNC_000023.11:g.110
741228_110741229in
s429
GRCh38 (hg38)NC_000023.11ChrX110,741,228110,741,228
nssv17741968RemappedPerfectNC_000023.10:g.109
984456_109984457in
s429
GRCh37.p13First PassNC_000023.10ChrX109,984,456109,984,456

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)
nssv17741968<0.00104006
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