A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213754



Internal ID20780794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:163184401..163192200hg38UCSC Ensembl
chr4:164105553..164113352hg19UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg387800
hg197800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6377384
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213754
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