A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12646n54



Internal ID20146070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:30374649..30698144hg38UCSC Ensembl
chr9:30374647..30698142hg19UCSC Ensembl
chr9:30364647..30688142hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38323496
hg19323496
hg18323496
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv614090, nsv614097
Samples
Known GenesLOC401497
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12646n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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