A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17710581



Internal ID134247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:90047900..90106682hg38UCSC Ensembl
chr16:90114308..90173090hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3858783
hg1958783
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5516739
Supporting Variants
Samples
Known GenesPRDM7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17710581
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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