A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978926



Internal ID12979351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:81759510..81965310hg38UCSC Ensembl
Innerchr11:81470552..81676352hg19UCSC Ensembl
Innerchr11:81148200..81354000hg18UCSC Ensembl
Innerchr11:81148200..81354000hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38205801
hg19205801
hg18205801
hg17205801
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)essv6978926
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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