A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15819619



Internal ID5398078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:24042801..24052866hg38UCSC Ensembl
chr18:21622765..21632830hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3810066
hg1910066
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3641975
Supporting Variants
SamplesNA18942
Known GenesTTC39C
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15819619
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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