A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979809



Internal ID12980793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:81628010..81718110hg38UCSC Ensembl
Innerchr11:81339052..81429152hg19UCSC Ensembl
Innerchr11:81016700..81106800hg18UCSC Ensembl
Innerchr11:81016700..81106800hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3890101
hg1990101
hg1890101
hg1790101
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34835
Supporting Variants
SamplesNA18633
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979809
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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