A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12656n54



Internal ID22780551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:31842564..31892859hg38UCSC Ensembl
chr9:31842562..31892857hg19UCSC Ensembl
chr9:31832562..31882857hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3850296
hg1950296
hg1850296
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv614134, nsv614133
Samples1780854449_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12656n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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