A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790444



Internal ID19173880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:52943795..53168503hg38UCSC Ensembl
Innerchr10:54703555..54928263hg19UCSC Ensembl
Innerchr10:54373561..54598269hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38224709
hg19224709
hg18224709
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891810
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=65
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790444
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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