A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636608



Internal ID7023402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:57350435..57426987hg38UCSC Ensembl
chr15:57642633..57719185hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3876553
hg1976553
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15259343, essv15259344, essv15259345
SamplesHG02661, NA20890, NA11919
Known GenesCGNL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636608
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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