A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638034



Internal ID6678132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:15452414..15620071hg38UCSC Ensembl
chr16:15546271..15713928hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38167658
hg19167658
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15385621, essv15385620, essv15385619
SamplesHG00334, HG03072, HG03890
Known GenesC16orf45, KIAA0430, MIR6506
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638034
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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