A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638754



Internal ID7025539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:59945099..59955205hg38UCSC Ensembl
chr16:59979003..59989109hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3810107
hg1910107
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15492885, essv15492884
SamplesNA21119, NA20849
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638754
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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