A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984071



Internal ID12630953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:62012552..62128252hg38UCSC Ensembl
Innerchr11:61780024..61895724hg19UCSC Ensembl
Innerchr11:61536600..61652300hg18UCSC Ensembl
Innerchr11:61536600..61652300hg17UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38115701
hg19115701
hg18115701
hg17115701
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751033
Supporting Variants
SamplesBEC_768
Known GenesINCENP
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6984071
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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