A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789473



Internal ID18835053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:12197945..12327862hg38UCSC Ensembl
Innerchr10:12239944..12369861hg19UCSC Ensembl
Innerchr10:12279950..12409867hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38129918
hg19129918
hg18129918
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891757
Supporting Variants
Samples
Known GenesCDC123
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=36
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789473
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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