A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16984708



Internal ID57193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42936096..42936174hg38UCSC Ensembl
chr6:42903834..42903912hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6141032
Supporting Variants
Samples
Known GenesCNPY3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16984708
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.071635


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