A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15955826



Internal ID6020660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:79022633..79067833hg38UCSC Ensembl
chr18:76782633..76827833hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3845201
hg1945201
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643285
Supporting Variants
SamplesNA19431
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15955826
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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