A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv500e214



Internal ID22756394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:27065722..27095642hg38UCSC Ensembl
chr16:27077043..27106963hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3829921
hg1929921
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3638317, esv3638316
SamplesNA18606, HG02266, HG01510
Known GenesC16orf82
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv500e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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