A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604012



Internal ID16391421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:78810125..78815124hg38UCSC Ensembl
Innerchr6:79519842..79524841hg19UCSC Ensembl
Innerchr6:79576561..79581560hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg385000
hg195000
hg185000
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10820n54
Supporting Variantsnssv1066954
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604012
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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