A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603394



Internal ID16390803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:64556214..64646490hg38UCSC Ensembl
Innerchr6:65266107..65356383hg19UCSC Ensembl
Innerchr6:65322828..65413104hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3890277
hg1990277
hg1890277
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154318
Samples1780854576_A
Known GenesEYS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603394
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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