A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981634



Internal ID12625743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:24161802..24544902hg38UCSC Ensembl
Innerchr9:24161800..24544900hg19UCSC Ensembl
Innerchr9:24151800..24534900hg18UCSC Ensembl
Innerchr9:24151800..24534900hg17UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38383101
hg19383101
hg18383101
hg17383101
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)essv6981634
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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