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nsv5427168

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:84

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 103 SVs from 21 studies. See in: genome view    
Submitted genomic156,892,730-156,892,813Question Mark
Overlapping variant regions from other studies: 109 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):156,862,522-156,862,605Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5427168Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1156,892,730156,892,813
nsv5427168RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1156,862,522156,862,605

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16890934deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16890934Submitted genomicNC_000001.11:g.156
892730_156892813de
l
GRCh38 (hg38)NC_000001.11Chr1156,892,730156,892,813
nssv16890934RemappedPerfectNC_000001.10:g.156
862522_156862605de
l
GRCh37.p13First PassNC_000001.10Chr1156,862,522156,862,605

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)
nssv16890934<0.00146404
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