A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642135



Internal ID6682216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:31792111..31849505hg38UCSC Ensembl
chr18:29372074..29429468hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3857395
hg1957395
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15837702
SamplesHG02292
Known GenesTRAPPC8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642135
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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