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nsv5411612

  • 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: 139 SVs from 20 studies. See in: genome view    
Submitted genomic177,354,677-177,354,728Question Mark
Overlapping variant regions from other studies: 141 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):177,323,813-177,323,864Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5411612Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1177,354,677177,354,728
nsv5411612RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1177,323,813177,323,864

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16892306alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16892306Submitted genomicNC_000001.11:g.177
354677_177354728in
s281
GRCh38 (hg38)NC_000001.11Chr1177,354,677177,354,728
nssv16892306RemappedPerfectNC_000001.10:g.177
323813_177323864in
s281
GRCh37.p13First PassNC_000001.10Chr1177,323,813177,323,864

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)
nssv16892306<0.00116404
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