A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613824



Internal ID16401233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:23405250..23515023hg38UCSC Ensembl
Innerchr9:23405248..23515021hg19UCSC Ensembl
Innerchr9:23395248..23505021hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38109774
hg19109774
hg18109774
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1131819
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613824
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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