A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988320



Internal ID12982123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5623811..5656021hg38UCSC Ensembl
Innerchr10:5665774..5697984hg19UCSC Ensembl
Innerchr10:5705780..5737990hg18UCSC Ensembl
Innerchr10:5705780..5737990hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3832211
hg1932211
hg1832211
hg1732211
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 Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988320
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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