A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202664



Internal ID20769704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:223478907..223478987hg38UCSC Ensembl
chr1:223652249..223652329hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6325696
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202664
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00015


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