A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636622



Internal ID7023416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58095010..58125126hg38UCSC Ensembl
chr15:58387209..58417325hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3830117
hg1930117
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15260047, essv15260046, essv15260045
SamplesNA19020, HG01498, NA19431
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636622
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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