A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791912



Internal ID19170575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:61112818..61146485hg38UCSC Ensembl
Innerchr18:58780051..58813718hg19UCSC Ensembl
Innerchr18:56931031..56964698hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3833668
hg1933668
hg1833668
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893110
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791912
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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