A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16985932



Internal ID58037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52995787..52995970hg38UCSC Ensembl
chr6:52860585..52860768hg19UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5473779
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16985932
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.019393


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