A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204991



Internal ID20772031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:30204029..30209996hg38UCSC Ensembl
chr22:30600018..30605985hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg385968
hg195968
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6545074
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204991
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