A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215029



Internal ID20782069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95440173..95440696hg38UCSC Ensembl
chr5:94775877..94776400hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38524
hg19524
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6408169
Supporting Variants
Samples
Known GenesFAM81B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215029
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