A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989569



Internal ID12974419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97166041..97214025hg38UCSC Ensembl
Innerchr11:97037041..97085025hg19UCSC Ensembl
Innerchr11:96542251..96590235hg18UCSC Ensembl
Innerchr11:96542251..96590235hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3847985
hg1947985
hg1847985
hg1747985
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751037
Supporting Variants
SamplesBEC_519
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989569
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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