A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6986698



Internal ID12979081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:21245161..21322661hg38UCSC Ensembl
Innerchr13:21819300..21896800hg19UCSC Ensembl
Innerchr13:20717300..20794800hg18UCSC Ensembl
Innerchr13:20717300..20794800hg17UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3877501
hg1977501
hg1877501
hg1777501
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34670
Supporting Variants
SamplesNA12236
Known GenesLINC00539, MIPEPP3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6986698
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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