A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6986896



Internal ID12633720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:245706..317370hg38UCSC Ensembl
Innerchr9:245706..317370hg19UCSC Ensembl
Innerchr9:235706..307370hg18UCSC Ensembl
Innerchr9:235706..307370hg17UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3871665
hg1971665
hg1871665
hg1771665
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34714
Supporting Variants
SamplesNA18572
Known GenesDOCK8
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6986896
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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