A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6990242



Internal ID12635362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133531889..133621047hg38UCSC Ensembl
Innerchr10:135345393..135434551hg19UCSC Ensembl
Innerchr10:135195383..135284541hg18UCSC Ensembl
Innerchr10:135234274..135323432hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3889159
hg1989159
hg1889159
hg1789159
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34487
Supporting Variants
SamplesNA19119
Known GenesCYP2E1, SPRNP1, SYCE1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6990242
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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