A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196623



Internal ID20763663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:39642012..39661059hg38UCSC Ensembl
chr18:37221976..37241023hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3819048
hg1919048
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6534453
Supporting Variants
Samples
Known GenesLINC00669
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196623
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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