A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790687



Internal ID18825157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87404437..87725505hg38UCSC Ensembl
Innerchr10:89164194..89485262hg19UCSC Ensembl
Innerchr10:89154174..89475242hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38321069
hg19321069
hg18321069
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891880
Supporting Variants
Samples
Known GenesLINC00864, MINPP1, MIR4678, PAPSS2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=92
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790687
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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