A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2751540



Internal ID12985092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:87220217..87335372hg38UCSC Ensembl
Innerchr15:87763448..87878603hg19UCSC Ensembl
Innerchr15:85564452..85679607hg18UCSC Ensembl
Innerchr15:85564452..85679607hg17UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38115156
hg19115156
hg18115156
hg17115156
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv111e55
Supporting Variantsessv6984781, essv6990023
SamplesSPC_179
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)esv2751540
Frequency
Sample Size771
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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