A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2752275



Internal ID12985827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11224627..11583747hg38UCSC Ensembl
Innerchr9:11224627..11583747hg19UCSC Ensembl
Innerchr9:11214627..11573747hg18UCSC Ensembl
Innerchr9:11214627..11573747hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38359121
hg19359121
hg18359121
hg17359121
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6987978, essv6981533, essv6989247, essv6987979, essv6981532, essv6981531
SamplesBEC_293
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)esv2752275
Frequency
Sample Size771
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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