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nsv5400744

  • 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: 109 SVs from 26 studies. See in: genome view    
Submitted genomic180,246,865-180,246,916Question Mark
Overlapping variant regions from other studies: 109 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):179,673,865-179,673,916Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5400744Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5180,246,865180,246,916
nsv5400744RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5179,673,865179,673,916

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16977752alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16977752Submitted genomicNC_000005.10:g.180
246865_180246916in
s281
GRCh38 (hg38)NC_000005.10Chr5180,246,865180,246,916
nssv16977752RemappedPerfectNC_000005.9:g.1796
73865_179673916ins
281
GRCh37.p13First PassNC_000005.9Chr5179,673,865179,673,916

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)
nssv16977752<0.00146404
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