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nsv5543270

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:43

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 258 SVs from 21 studies. See in: genome view    
Submitted genomic110,705,440-110,705,482Question Mark
Overlapping variant regions from other studies: 258 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):109,948,668-109,948,710Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5543270Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX110,705,440110,705,482
nsv5543270RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX109,948,668109,948,710

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17741966insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17741966Submitted genomicNC_000023.11:g.110
705440_110705482in
s143
GRCh38 (hg38)NC_000023.11ChrX110,705,440110,705,482
nssv17741966RemappedPerfectNC_000023.10:g.109
948668_109948710in
s143
GRCh37.p13First PassNC_000023.10ChrX109,948,668109,948,710

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)
nssv177419660.49931956404
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