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nsv5421459

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:120

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 113 SVs from 20 studies. See in: genome view    
Submitted genomic160,134,085-160,134,204Question Mark
Overlapping variant regions from other studies: 117 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):160,103,875-160,103,994Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5421459Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1160,134,085160,134,204
nsv5421459RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1160,103,875160,103,994

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16891357deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16891357Submitted genomicNC_000001.11:g.160
134085_160134204de
l
GRCh38 (hg38)NC_000001.11Chr1160,134,085160,134,204
nssv16891357RemappedPerfectNC_000001.10:g.160
103875_160103994de
l
GRCh37.p13First PassNC_000001.10Chr1160,103,875160,103,994

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)
nssv16891357<0.00136404
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