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nsv5436654

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,241

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 194 SVs from 35 studies. See in: genome view    
Submitted genomic182,807,888-182,813,128Question Mark
Overlapping variant regions from other studies: 196 SVs from 35 studies. See in: genome view    
Remapped(Score: Perfect):182,777,023-182,782,263Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5436654Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1182,807,888182,813,128
nsv5436654RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1182,777,023182,782,263

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16892826deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16892826Submitted genomicNC_000001.11:g.182
807888_182813128de
l
GRCh38 (hg38)NC_000001.11Chr1182,807,888182,813,128
nssv16892826RemappedPerfectNC_000001.10:g.182
777023_182782263de
l
GRCh37.p13First PassNC_000001.10Chr1182,777,023182,782,263

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)
nssv168928260.002116404
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