A curated catalogue of human genomic structural variation




Variant Details

Variant: esv34677



Internal ID12644027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90079272..90249274hg38UCSC Ensembl
Innerchr15:90622504..90792506hg19UCSC Ensembl
Innerchr15:88423508..88593510hg18UCSC Ensembl
Innerchr15:88423508..88593510hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38170003
hg19170003
hg18170003
hg17170003
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv112e55
Supporting Variantsessv6978406, essv6978407, essv6990234, essv6986609
SamplesNA19093
Known GenesCIB1, GDPGP1, IDH2, SEMA4B, ZNF710
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)esv34677
Frequency
Sample Size771
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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