A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980916



Internal ID12982289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4141247..4213518hg38UCSC Ensembl
Innerchr11:4162477..4234748hg19UCSC Ensembl
Innerchr11:4119053..4191324hg18UCSC Ensembl
Innerchr11:4119053..4191324hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3872272
hg1972272
hg1872272
hg1772272
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34983
Supporting Variants
SamplesNA19144
Known GenesLOC100506082
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980916
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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