A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788210



Internal ID18825571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5269112..5354365hg38UCSC Ensembl
Innerchr10:5311075..5396328hg19UCSC Ensembl
Innerchr10:5301075..5386328hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3885254
hg1985254
hg1885254
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891744
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=35
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788210
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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