A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635818



Internal ID7022616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:23001917..23024466hg38UCSC Ensembl
chr15:22848602..22871151hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3822550
hg1922550
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15176400, essv15176404, essv15176402, essv15176411, essv15176409, essv15176413, essv15176410, essv15176412, essv15176406, essv15176401, essv15176408, essv15176405, essv15176407, essv15176403
SamplesHG02973, HG04002, HG02792, NA20814, HG03640, HG03937, HG02603, HG02597, HG00657, NA18555, HG02184, HG01113, HG01395, NA21091
Known GenesTUBGCP5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635818
Frequency
Sample Size2504
Observed Gain14
Observed Loss0
Observed Complex0
Frequencyn/a


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