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nsv5426369

  • 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: 90 SVs from 21 studies. See in: genome view    
Submitted genomic41,034,617-41,034,668Question Mark
Overlapping variant regions from other studies: 90 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):41,326,815-41,326,866Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5426369Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1541,034,61741,034,668
nsv5426369RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1541,326,81541,326,866

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17700157alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17700157Submitted genomicNC_000015.10:g.410
34617_41034668ins2
80
GRCh38 (hg38)NC_000015.10Chr1541,034,61741,034,668
nssv17700157RemappedPerfectNC_000015.9:g.4132
6815_41326866ins28
0
GRCh37.p13First PassNC_000015.9Chr1541,326,81541,326,866

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)
nssv17700157<0.00156404
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