A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605339



Internal ID16392748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167190659..167214272hg38UCSC Ensembl
Innerchr6:167604147..167627760hg19UCSC Ensembl
Innerchr6:167524137..167547750hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3823614
hg1923614
hg1823614
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154897
Samples1780854477_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605339
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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