A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604013



Internal ID16391422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:78810125..78815149hg38UCSC Ensembl
Innerchr6:79519842..79524866hg19UCSC Ensembl
Innerchr6:79576561..79581585hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg385025
hg195025
hg185025
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10820n54
Supporting Variantsnssv1066955
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604013
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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