A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2751033



Internal ID12637899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:62012550..62128252hg38UCSC Ensembl
Innerchr11:61780022..61895724hg19UCSC Ensembl
Innerchr11:61536598..61652300hg18UCSC Ensembl
Innerchr11:61536598..61652300hg17UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38115703
hg19115703
hg18115703
hg17115703
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6984070, essv6984071
SamplesBEC_768
Known GenesINCENP
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv2751033
Frequency
Sample Size771
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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