A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6990234



Internal ID12635239
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 StatusS
Merged Variantsesv34677
Supporting Variants
SamplesNA19093
Known GenesCIB1, GDPGP1, IDH2, SEMA4B, ZNF710
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6990234
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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