A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1061464



Internal ID15914650
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 StatusS
Merged Variantsnsv603376
Supporting Variants
Samples
Known GenesEYS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1061464
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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