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nsv5431006

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,234

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 191 SVs from 40 studies. See in: genome view    
Submitted genomic113,097,541-113,098,774Question Mark
Overlapping variant regions from other studies: 192 SVs from 40 studies. See in: genome view    
Remapped(Score: Perfect):113,640,163-113,641,396Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5431006Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1113,097,541113,098,774
nsv5431006RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1113,640,163113,641,396

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16908102deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16908102Submitted genomicNC_000001.11:g.113
097541_113098774de
l
GRCh38 (hg38)NC_000001.11Chr1113,097,541113,098,774
nssv16908102RemappedPerfectNC_000001.10:g.113
640163_113641396de
l
GRCh37.p13First PassNC_000001.10Chr1113,640,163113,641,396

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)
nssv16908102<0.00116404
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