A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16982602



Internal ID55765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:53715479..53726379hg38UCSC Ensembl
chr6:53580277..53591177hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3810901
hg1910901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5464636
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16982602
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000781


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