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nsv5423108

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:74

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 119 SVs from 26 studies. See in: genome view    
Submitted genomic46,294,518-46,294,591Question Mark
Overlapping variant regions from other studies: 119 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):46,760,190-46,760,263Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5423108Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr146,294,51846,294,591
nsv5423108RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr146,760,19046,760,263

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16901851deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16901851Submitted genomicNC_000001.11:g.462
94518_46294591del
GRCh38 (hg38)NC_000001.11Chr146,294,51846,294,591
nssv16901851RemappedPerfectNC_000001.10:g.467
60190_46760263del
GRCh37.p13First PassNC_000001.10Chr146,760,19046,760,263

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)
nssv16901851<0.00146404
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