A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605573



Internal ID16392982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:170458953..170470178hg38UCSC Ensembl
Innerchr6:170768041..170779266hg19UCSC Ensembl
Innerchr6:170609966..170621191hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3811226
hg1911226
hg1811226
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1077578
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605573
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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