A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211794



Internal ID20778834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2518676..2523441hg38UCSC Ensembl
chr4:2520403..2525168hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg384766
hg194766
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367949
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211794
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