A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2752272



Internal ID12985824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:102077075..102199578hg38UCSC Ensembl
Innerchr9:104839357..104961860hg19UCSC Ensembl
Innerchr9:103879178..104001681hg18UCSC Ensembl
Innerchr9:101918912..102041415hg17UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38122504
hg19122504
hg18122504
hg17122504
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6989459, essv6984874, essv6990035, essv6984873
SamplesSPC_188
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)esv2752272
Frequency
Sample Size771
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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