A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789461



Internal ID19169020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:42268371..42320898hg38UCSC Ensembl
Innerchr18:39848336..39900863hg19UCSC Ensembl
Innerchr18:38102334..38154861hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3852528
hg1952528
hg1852528
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893098
Supporting Variants
Samples
Known GenesLINC00907
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=13
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789461
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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