A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2897n223



Internal ID22805865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:60520301..60540500hg38UCSC Ensembl
chr16:60554205..60574404hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3820200
hg1920200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6504017, nsv6513309, nsv6511143, nsv6508944, nsv6498797
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2897n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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