A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985622



Internal ID12625737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:24138908..24544895hg38UCSC Ensembl
Innerchr9:24138906..24544893hg19UCSC Ensembl
Innerchr9:24128906..24534893hg18UCSC Ensembl
Innerchr9:24128906..24534893hg17UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38405988
hg19405988
hg18405988
hg17405988
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752290
Supporting Variants
SamplesBEC_309
Known GenesIZUMO3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985622
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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