A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212098



Internal ID20779138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:151371864..151449207hg38UCSC Ensembl
chr4:152293016..152370359hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3877344
hg1977344
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6391647
Supporting Variants
Samples
Known GenesFAM160A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212098
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