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nsv5425323

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:72

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 136 SVs from 24 studies. See in: genome view    
Submitted genomic112,645,236-112,645,307Question Mark
Overlapping variant regions from other studies: 137 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):113,187,858-113,187,929Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5425323Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1112,645,236112,645,307
nsv5425323RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1113,187,858113,187,929

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16908923deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16908923Submitted genomicNC_000001.11:g.112
645236_112645307de
l
GRCh38 (hg38)NC_000001.11Chr1112,645,236112,645,307
nssv16908923RemappedPerfectNC_000001.10:g.113
187858_113187929de
l
GRCh37.p13First PassNC_000001.10Chr1113,187,858113,187,929

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)
nssv16908923<0.00116404
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