A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792748



Internal ID19161887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87571434..87629821hg38UCSC Ensembl
Innerchr10:89331191..89389578hg19UCSC Ensembl
Innerchr10:89321171..89379558hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3858388
hg1958388
hg1858388
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891881
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=22
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792748
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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