A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1067377



Internal ID15920563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:82813965..82849690hg38UCSC Ensembl
Innerchr6:83523684..83559409hg19UCSC Ensembl
Innerchr6:83580403..83616128hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3835726
hg1935726
hg1835726
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604090
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)nssv1067377
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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