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nsv5424656

  • 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: 162 SVs from 38 studies. See in: genome view    
Submitted genomic63,873,061-63,873,112Question Mark
Overlapping variant regions from other studies: 162 SVs from 38 studies. See in: genome view    
Remapped(Score: Perfect):62,504,414-62,504,465Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5424656Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2063,873,06163,873,112
nsv5424656RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2062,504,41462,504,465

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17733704alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17733704Submitted genomicNC_000020.11:g.638
73061_63873112ins2
80
GRCh38 (hg38)NC_000020.11Chr2063,873,06163,873,112
nssv17733704RemappedPerfectNC_000020.10:g.625
04414_62504465ins2
80
GRCh37.p13First PassNC_000020.10Chr2062,504,41462,504,465

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)
nssv177337040.0362206188
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