A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225677



Internal ID20792717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:23101404..23103924hg38UCSC Ensembl
chr6:23101632..23104152hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg382521
hg192521
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6413486
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225677
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00171


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