A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2751035



Internal ID12637901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:8410107..8663904hg38UCSC Ensembl
Innerchr11:8431654..8685451hg19UCSC Ensembl
Innerchr11:8388230..8642027hg18UCSC Ensembl
Innerchr11:8388230..8642027hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38253798
hg19253798
hg18253798
hg17253798
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6989839, essv6989385, essv6983673, essv6983674, essv6983672
SamplesBEC_611
Known GenesSTK33, TRIM66
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)esv2751035
Frequency
Sample Size771
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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