A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15900102



Internal ID5841034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:61470406..61485339hg38UCSC Ensembl
chr18:59137639..59152572hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3814934
hg1914934
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3642731
Supporting Variants
SamplesNA19213
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15900102
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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