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nsv5422627

  • 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: 94 SVs from 19 studies. See in: genome view    
Submitted genomic72,442,201-72,442,252Question Mark
Overlapping variant regions from other studies: 94 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):70,438,341-70,438,392Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5422627Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1772,442,20172,442,252
nsv5422627RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1770,438,34170,438,392

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17714429alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17714429Submitted genomicNC_000017.11:g.724
42201_72442252ins2
81
GRCh38 (hg38)NC_000017.11Chr1772,442,20172,442,252
nssv17714429RemappedPerfectNC_000017.10:g.704
38341_70438392ins2
81
GRCh37.p13First PassNC_000017.10Chr1770,438,34170,438,392

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)
nssv17714429<0.00146404
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