A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638726



Internal ID7025511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58443451..58462267hg38UCSC Ensembl
chr16:58477355..58496171hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3818817
hg1918817
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15486840, essv15486838, essv15486839
SamplesNA12286, NA19036, HG01669
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638726
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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