A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2959n223



Internal ID22805927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87251853..87314005hg38UCSC Ensembl
chr16:87285459..87347611hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3862153
hg1962153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6514016, nsv6508762
Samples
Known GenesC16orf95, LOC101928682
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2959n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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