A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639408



Internal ID6679501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84011958..84093765hg38UCSC Ensembl
chr16:84045563..84127370hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3881808
hg1981808
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv546e214
Supporting Variantsessv15545788, essv15545789, essv15545790
SamplesHG03965, HG03717, HG02685
Known GenesMBTPS1, SLC38A8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639408
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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