A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210223



Internal ID20777263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:121696201..121697800hg38UCSC Ensembl
chr4:122617356..122618955hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6378140
Supporting Variants
Samples
Known GenesANXA5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210223
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