A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979577



Internal ID12633705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:46431..279753hg38UCSC Ensembl
Innerchr9:46431..279753hg19UCSC Ensembl
Innerchr9:36431..269753hg18UCSC Ensembl
Innerchr9:36431..269753hg17UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38233323
hg19233323
hg18233323
hg17233323
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34714
Supporting Variants
SamplesNA18572
Known GenesC9orf66, CBWD1, DOCK8, FOXD4
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979577
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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