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nsv5400144

  • 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: 158 SVs from 24 studies. See in: genome view    
Submitted genomic177,957,338-177,957,389Question Mark
Overlapping variant regions from other studies: 160 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):177,926,473-177,926,524Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5400144Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1177,957,338177,957,389
nsv5400144RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1177,926,473177,926,524

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16892633alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16892633Submitted genomicNC_000001.11:g.177
957338_177957389in
s271
GRCh38 (hg38)NC_000001.11Chr1177,957,338177,957,389
nssv16892633RemappedPerfectNC_000001.10:g.177
926473_177926524in
s271
GRCh37.p13First PassNC_000001.10Chr1177,926,473177,926,524

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)
nssv168926330.00176404
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