A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2750868



Internal ID12637734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133381434..133621047hg38UCSC Ensembl
Innerchr10:135194938..135434551hg19UCSC Ensembl
Innerchr10:135044928..135284541hg18UCSC Ensembl
Innerchr10:135083819..135323432hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38239614
hg19239614
hg18239614
hg17239614
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv35e55
Supporting Variantsessv6988740, essv6987469, essv6987468, essv6983990, essv6983989
SamplesBEC_740
Known GenesCYP2E1, MTG1, PAOX, SCART1, SPRN, SPRNP1, SYCE1
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)esv2750868
Frequency
Sample Size771
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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