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nsv5423922

  • 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: 165 SVs from 19 studies. See in: genome view    
Submitted genomic35,475,906-35,475,957Question Mark
Overlapping variant regions from other studies: 165 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):33,055,870-33,055,921Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5423922Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1835,475,90635,475,957
nsv5423922RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1833,055,87033,055,921

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17717311alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17717311Submitted genomicNC_000018.10:g.354
75906_35475957ins2
81
GRCh38 (hg38)NC_000018.10Chr1835,475,90635,475,957
nssv17717311RemappedPerfectNC_000018.9:g.3305
5870_33055921ins28
1
GRCh37.p13First PassNC_000018.9Chr1833,055,87033,055,921

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)
nssv177173110.003206404
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