A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614146



Internal ID16054869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33186158..33398608hg38UCSC Ensembl
Innerchr9:33186156..33398606hg19UCSC Ensembl
Innerchr9:33176156..33388606hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38212451
hg19212451
hg18212451
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1132839
Samples
Known GenesAQP7, BAG1, CHMP5, NFX1, SPINK4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614146
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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