A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17707595



Internal ID131261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:29410486..29424486hg38UCSC Ensembl
chr16:29421807..29435807hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3814001
hg1914001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5524027
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17707595
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003096


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