A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613655



Internal ID16401064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:15602103..15670447hg38UCSC Ensembl
Innerchr9:15602101..15670445hg19UCSC Ensembl
Innerchr9:15592101..15660445hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3868345
hg1968345
hg1868345
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1128805
Samples
Known GenesCCDC171
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613655
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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