A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15810999



Internal ID5578473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:12045353..12076109hg38UCSC Ensembl
chr18:12045352..12076108hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3830757
hg1930757
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3641827
Supporting Variants
SamplesNA19023
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15810999
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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