A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978883



Internal ID12979291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:81759510..82022910hg38UCSC Ensembl
Innerchr11:81470552..81733952hg19UCSC Ensembl
Innerchr11:81148200..81411600hg18UCSC Ensembl
Innerchr11:81148200..81411600hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38263401
hg19263401
hg18263401
hg17263401
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)essv6978883
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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