A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213325



Internal ID20780365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:109876875..109885927hg38UCSC Ensembl
chr5:109212576..109221628hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg389053
hg199053
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6410335
Supporting Variants
Samples
Known GenesLOC100289673
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213325
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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