A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15851822



Internal ID2003651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:41196974..41358657hg38UCSC Ensembl
chr18:38776938..38938621hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg38161684
hg19161684
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3642317
Supporting Variants
SamplesHG01852
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15851822
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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