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nsv5394391

  • 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: 161 SVs from 27 studies. See in: genome view    
Submitted genomic177,955,148-177,955,199Question Mark
Overlapping variant regions from other studies: 163 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):177,924,283-177,924,334Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5394391Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1177,955,148177,955,199
nsv5394391RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1177,924,283177,924,334

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16892631alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16892631Submitted genomicNC_000001.11:g.177
955148_177955199in
s250
GRCh38 (hg38)NC_000001.11Chr1177,955,148177,955,199
nssv16892631RemappedPerfectNC_000001.10:g.177
924283_177924334in
s250
GRCh37.p13First PassNC_000001.10Chr1177,924,283177,924,334

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)
nssv168926310.013836404
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