A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212657



Internal ID20779697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:105121090..105698274hg38UCSC Ensembl
chr5:104456791..105033975hg19UCSC Ensembl
Cytoband5q21.2
Allele length
AssemblyAllele length
hg38577185
hg19577185
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6406021
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212657
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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