A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603376



Internal ID16390785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:63879572..64061449hg38UCSC Ensembl
Innerchr6:64589465..64771342hg19UCSC Ensembl
Innerchr6:64647424..64829301hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38181878
hg19181878
hg18181878
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1061464
Samples
Known GenesEYS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603376
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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