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nsv5423587

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,689

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 181 SVs from 31 studies. See in: genome view    
Submitted genomic177,977,110-177,982,798Question Mark
Overlapping variant regions from other studies: 183 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):177,946,245-177,951,933Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5423587Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1177,977,110177,982,798
nsv5423587RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1177,946,245177,951,933

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16892637deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16892637Submitted genomicNC_000001.11:g.177
977110_177982798de
l
GRCh38 (hg38)NC_000001.11Chr1177,977,110177,982,798
nssv16892637RemappedPerfectNC_000001.10:g.177
946245_177951933de
l
GRCh37.p13First PassNC_000001.10Chr1177,946,245177,951,933

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)
nssv16892637<0.00126404
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