A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214560



Internal ID20781601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:119439901..119445200hg38UCSC Ensembl
chr6:119761066..119766365hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg385300
hg195300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6609120
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214560
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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