A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215436



Internal ID20782476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:96519151..96538869hg38UCSC Ensembl
chr5:95854855..95874573hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3819719
hg1919719
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6407286
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215436
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