A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16977919



Internal ID52680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:67000..136000hg38UCSC Ensembl
chr6:67000..136000hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3869001
hg1969001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6141006
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16977919
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001209


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer