A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790473



Internal ID19178674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:107529838..108298389hg38UCSC Ensembl
Innerchr10:109289596..110058147hg19UCSC Ensembl
Innerchr10:109279586..110048137hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38768552
hg19768552
hg18768552
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891889
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=184
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790473
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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