A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789089



Internal ID18818023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:63812857..63849506hg38UCSC Ensembl
Innerchr18:61480091..61516740hg19UCSC Ensembl
Innerchr18:59631071..59667720hg18UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3836650
hg1936650
hg1836650
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893113
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=12
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789089
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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