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nsv5564128

  • 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 22 studies. See in: genome view    
Submitted genomic180,321,743-180,321,794Question Mark
Overlapping variant regions from other studies: 90 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):180,039,531-180,039,582Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5564128Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3180,321,743180,321,794
nsv5564128RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3180,039,531180,039,582

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17735021line1 insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17735021Submitted genomicNC_000003.12:g.180
321743_180321794in
s854
GRCh38 (hg38)NC_000003.12Chr3180,321,743180,321,794
nssv17735021RemappedPerfectNC_000003.11:g.180
039531_180039582in
s854
GRCh37.p13First PassNC_000003.11Chr3180,039,531180,039,582

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)
nssv17735021<0.00136402
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