A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7484n100



Internal ID22793571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:26242028..26434484hg38UCSC Ensembl
chr9:26242026..26434482hg19UCSC Ensembl
chr9:26232026..26424482hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38192457
hg19192457
hg18192457
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1018547, nsv1027596, nsv1033265, nsv1016727
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7484n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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