A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799574



Internal ID19178393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:40934412..40968819hg38UCSC Ensembl
Innerchr18:38514376..38548783hg19UCSC Ensembl
Innerchr18:36768374..36802781hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3834408
hg1934408
hg1834408
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893096
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799574
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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