A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25783214



Internal ID19174115
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 HumanHap 610
CommentsNumber of probes=32
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25783214
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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