A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603250



Internal ID16390659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:61265212..61345562hg38UCSC Ensembl
Innerchr6:61891638..61972502hg19UCSC Ensembl
Innerchr6:61949597..62030461hg18UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg3880351
hg1980865
hg1880865
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1061058
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603250
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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