A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209520



Internal ID20776560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:109701801..109705800hg38UCSC Ensembl
chr4:110622957..110626956hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg384000
hg194000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6395418
Supporting Variants
Samples
Known GenesCASP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209520
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