A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16985192



Internal ID57524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:97779395..97785000hg38UCSC Ensembl
chr6:98227271..98232876hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg385606
hg195606
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5461063
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16985192
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00336


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