A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796331



Internal ID19169213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:69044336..69100794hg38UCSC Ensembl
Innerchr18:66711573..66768031hg19UCSC Ensembl
Innerchr18:64862553..64919011hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3856459
hg1956459
hg1856459
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893130
Supporting Variants
Samples
Known GenesCCDC102B
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=19
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796331
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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