A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639424



Internal ID6679517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84427606..84467733hg38UCSC Ensembl
chr16:84461212..84501339hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3840128
hg1940128
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15545871, essv15545872
SamplesHG02008, HG00362
Known GenesATP2C2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639424
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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