A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789234



Internal ID19173367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:2184723..2406367hg38UCSC Ensembl
Innerchr18:2184723..2406366hg19UCSC Ensembl
Innerchr18:2174723..2396366hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38221645
hg19221644
hg18221644
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893062
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=49
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789234
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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