A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603393



Internal ID16390802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:64544310..64633573hg38UCSC Ensembl
Innerchr6:65254203..65343466hg19UCSC Ensembl
Innerchr6:65310924..65400187hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3889264
hg1989264
hg1889264
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154317
SamplesHGDP01074
Known GenesEYS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603393
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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