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nsv5400732

  • 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: 96 SVs from 23 studies. See in: genome view    
Submitted genomic163,448,274-163,448,325Question Mark
Overlapping variant regions from other studies: 96 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):162,875,280-162,875,331Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5400732Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5163,448,274163,448,325
nsv5400732RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5162,875,280162,875,331

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16977023alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16977023Submitted genomicNC_000005.10:g.163
448274_163448325in
s265
GRCh38 (hg38)NC_000005.10Chr5163,448,274163,448,325
nssv16977023RemappedPerfectNC_000005.9:g.1628
75280_162875331ins
265
GRCh37.p13First PassNC_000005.9Chr5162,875,280162,875,331

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)
nssv16977023<0.00116404
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