A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17705867



Internal ID129533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:34161000..34168000hg38UCSC Ensembl
chr16:33963467..33970467hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg387001
hg197001
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5424537
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17705867
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.5


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