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nsv5427814

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:233

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 96 SVs from 15 studies. See in: genome view    
Submitted genomic151,776,694-151,776,926Question Mark
Overlapping variant regions from other studies: 107 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):151,749,170-151,749,402Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5427814Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1151,776,694151,776,926
nsv5427814RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1151,749,170151,749,402

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16890333deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16890333Submitted genomicNC_000001.11:g.151
776694_151776926de
l
GRCh38 (hg38)NC_000001.11Chr1151,776,694151,776,926
nssv16890333RemappedPerfectNC_000001.10:g.151
749170_151749402de
l
GRCh37.p13First PassNC_000001.10Chr1151,749,170151,749,402

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)
nssv16890333<0.00116404
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