A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17707696



Internal ID131362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30549906..30549989hg38UCSC Ensembl
chr16:30561227..30561310hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5514932
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17707696
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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