A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605209



Internal ID16045932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:163414249..163417980hg38UCSC Ensembl
Innerchr6:163835281..163839012hg19UCSC Ensembl
Innerchr6:163755271..163759002hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg383732
hg193732
hg183732
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1075617
Samples
Known GenesQKI
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605209
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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