A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978882



Internal ID12979292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:81759499..82022942hg38UCSC Ensembl
Innerchr11:81470541..81733984hg19UCSC Ensembl
Innerchr11:81148189..81411632hg18UCSC Ensembl
Innerchr11:81148189..81411632hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38263444
hg19263444
hg18263444
hg17263444
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34646
Supporting Variants
SamplesNA12753
Known GenesMIR4300
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978882
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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