A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17709885



Internal ID133551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:82010106..82015982hg38UCSC Ensembl
chr16:82043711..82049587hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg385877
hg195877
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5523194
Supporting Variants
Samples
Known GenesSDR42E1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17709885
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000625


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