A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604106



Internal ID16044829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:85995537..87138584hg38UCSC Ensembl
Innerchr6:86705255..87848302hg19UCSC Ensembl
Innerchr6:86761974..87905021hg18UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg381143048
hg191143048
hg181143048
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1067621
Samples
Known GenesCGA, HTR1E, MIR548AD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604106
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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