A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605240



Internal ID16392649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:164709839..164834807hg38UCSC Ensembl
Innerchr6:165130872..165248296hg19UCSC Ensembl
Innerchr6:165050862..165168286hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38124969
hg19117425
hg18117425
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1075798
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605240
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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