A curated catalogue of human genomic structural variation




Variant Details

Variant: esv34566



Internal ID12990603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7291742..7781370hg38UCSC Ensembl
Innerchr9:7291742..7781370hg19UCSC Ensembl
Innerchr9:7281742..7771370hg18UCSC Ensembl
Innerchr9:7281742..7771370hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38489629
hg19489629
hg18489629
hg17489629
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6987772, essv6980359, essv6980360, essv6987771, essv6980362, essv6980361
SamplesNA07345
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv34566
Frequency
Sample Size771
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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