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nsv5557239

  • 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: 259 SVs from 23 studies. See in: genome view    
Submitted genomic87,663,439-87,663,490Question Mark
Overlapping variant regions from other studies: 259 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):86,918,439-86,918,490Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5557239Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX87,663,43987,663,490
nsv5557239RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX86,918,43986,918,490

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17741276alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17741276Submitted genomicNC_000023.11:g.876
63439_87663490ins2
81
GRCh38 (hg38)NC_000023.11ChrX87,663,43987,663,490
nssv17741276RemappedPerfectNC_000023.10:g.869
18439_86918490ins2
81
GRCh37.p13First PassNC_000023.10ChrX86,918,43986,918,490

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)
nssv17741276<0.00156404
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