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nsv4517795

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:455,007

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 452 SVs from 18 studies. See in: genome view    
Remapped(Score: Good):116,924,031-117,379,037Question Mark
Overlapping variant regions from other studies: 448 SVs from 18 studies. See in: genome view    
Submitted genomic116,057,999-116,513,000Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4517795RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000023.11ChrX116,924,031117,379,037
nsv4517795Submitted genomicGRCh37.p13Primary AssemblyNC_000023.10ChrX116,057,999116,513,000

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15989260duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15989260RemappedGoodNC_000023.11:g.116
924031_117379037du
p
GRCh38.p12First PassNC_000023.11ChrX116,924,031117,379,037
nssv15989260Submitted genomicNC_000023.10:g.116
057999_116513000du
p
GRCh37.p13NC_000023.10ChrX116,057,999116,513,000

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)
nssv159892604.6e-005121694
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