A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16980861



Internal ID54609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27639790..27647580hg38UCSC Ensembl
chr6:27607569..27615359hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg387791
hg197791
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5462195
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16980861
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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