A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14087737



Internal ID21275708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:120740843..120763520hg38UCSC Ensembl
Innerchr6:121061989..121084666hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3822678
hg1922678
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115178
Supporting Variants
Samplessample226
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14087737
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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