A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12590n54



Internal ID22780485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:23171517..23186455hg38UCSC Ensembl
chr9:23171516..23186453hg19UCSC Ensembl
chr9:23161516..23176453hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3814939
hg1914938
hg1814938
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv613791, nsv613792
Samples1782681169_A, HGDP00019
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12590n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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