A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5932022



Internal ID22707314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67120788..67122341hg38UCSC Ensembl
chr16:67154691..67156244hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg381554
hg191554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17385085
Samples
Known GenesC16orf70
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5932022
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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