A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17707561



Internal ID131227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68331932..68332367hg38UCSC Ensembl
chr16:68365835..68366270hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38436
hg19436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5520426
Supporting Variants
Samples
Known GenesPRMT7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17707561
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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