A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638121



Internal ID7024907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19131300..19167136hg38UCSC Ensembl
chr16:19142622..19178458hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3835837
hg1935837
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv487e214
Supporting Variantsessv15398506, essv15398509, essv15398508, essv15398507
SamplesHG01366, HG01353, HG01498, HG01375
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638121
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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