A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1065570



Internal ID15918756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:77627089..77937031hg38UCSC Ensembl
Innerchr6:78336806..78646748hg19UCSC Ensembl
Innerchr6:78393525..78703467hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38309943
hg19309943
hg18309943
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv603812
Supporting Variants
Samples
Known GenesMEI4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1065570
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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