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nsv5396616

  • 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 23 studies. See in: genome view    
Submitted genomic183,515,617-183,515,668Question Mark
Overlapping variant regions from other studies: 90 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):183,233,405-183,233,456Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5396616Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3183,515,617183,515,668
nsv5396616RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3183,233,405183,233,456

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16944742alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16944742Submitted genomicNC_000003.12:g.183
515617_183515668in
s280
GRCh38 (hg38)NC_000003.12Chr3183,515,617183,515,668
nssv16944742RemappedPerfectNC_000003.11:g.183
233405_183233456in
s280
GRCh37.p13First PassNC_000003.11Chr3183,233,405183,233,456

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)
nssv16944742<0.00136404
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