A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1067373



Internal ID15573873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:81082696..81616374hg38UCSC Ensembl
Innerchr6:81792413..82326091hg19UCSC Ensembl
Innerchr6:81849132..82382810hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38533679
hg19533679
hg18533679
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604087
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1067373
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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