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nsv5406012

  • 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: 152 SVs from 21 studies. See in: genome view    
Submitted genomic177,968,696-177,968,747Question Mark
Overlapping variant regions from other studies: 154 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):177,937,831-177,937,882Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5406012Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1177,968,696177,968,747
nsv5406012RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1177,937,831177,937,882

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16892636alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16892636Submitted genomicNC_000001.11:g.177
968696_177968747in
s281
GRCh38 (hg38)NC_000001.11Chr1177,968,696177,968,747
nssv16892636RemappedPerfectNC_000001.10:g.177
937831_177937882in
s281
GRCh37.p13First PassNC_000001.10Chr1177,937,831177,937,882

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)
nssv16892636<0.00116404
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