A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16983808



Internal ID56581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:76708076..76793833hg38UCSC Ensembl
chr6:77417793..77503550hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3885758
hg1985758
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5467559
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16983808
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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