A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978925



Internal ID12979359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:81737473..82049063hg38UCSC Ensembl
Innerchr11:81448515..81760105hg19UCSC Ensembl
Innerchr11:81126163..81437753hg18UCSC Ensembl
Innerchr11:81126163..81437753hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38311591
hg19311591
hg18311591
hg17311591
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34312
Supporting Variants
SamplesNA12763
Known GenesMIR4300
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978925
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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