A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978927



Internal ID12979356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:81778010..82043810hg38UCSC Ensembl
Innerchr11:81489052..81754852hg19UCSC Ensembl
Innerchr11:81166700..81432500hg18UCSC Ensembl
Innerchr11:81166700..81432500hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38265801
hg19265801
hg18265801
hg17265801
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 Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978927
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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