A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7376690



Internal ID10308286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:79739851..79740211hg38UCSC Ensembl
Outerchr18:77499851..77500211hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38361
hg19361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3107123
Supporting Variants
SamplesHuRef
Known GenesCTDP1
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7376690
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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