A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2752293



Internal ID12985845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:28186823..28380169hg38UCSC Ensembl
Innerchr9:28186821..28380167hg19UCSC Ensembl
Innerchr9:28176821..28370167hg18UCSC Ensembl
Innerchr9:28176821..28370167hg17UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38193347
hg19193347
hg18193347
hg17193347
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv259e55
Supporting Variantsessv6984415, essv6989957
SamplesBEC_704
Known GenesLINGO2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv2752293
Frequency
Sample Size771
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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