A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980820



Internal ID12982140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5623811..5674895hg38UCSC Ensembl
Innerchr10:5665774..5716858hg19UCSC Ensembl
Innerchr10:5705780..5756864hg18UCSC Ensembl
Innerchr10:5705780..5756864hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3851085
hg1951085
hg1851085
hg1751085
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35082
Supporting Variants
SamplesNA19131
Known GenesASB13
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980820
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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