A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12619n54



Internal ID22780514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:26641559..26691670hg38UCSC Ensembl
chr9:26641557..26691668hg19UCSC Ensembl
chr9:26631557..26681668hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3850112
hg1950112
hg1850112
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv613939, nsv613940
SamplesHGDP01336, HGDP01330
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12619n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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