A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513802



Internal ID20887150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69527759..69530431hg38UCSC Ensembl
chr16:69561662..69564334hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg382673
hg192673
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031215
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513802
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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