A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv552e214



Internal ID22756446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87279310..87303441hg38UCSC Ensembl
chr16:87312916..87337047hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3824132
hg1924132
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3639508, esv3639507
SamplesHG03817, HG00284, HG00329, HG03894
Known GenesC16orf95, LOC101928682
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv552e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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