A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613829



Internal ID16401238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:23940422..24035013hg38UCSC Ensembl
Innerchr9:23940420..24035011hg19UCSC Ensembl
Innerchr9:23930420..24025011hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3894592
hg1994592
hg1894592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12597n54
Supporting Variantsnssv1131826
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613829
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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