A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177192



Internal ID20744232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:106536201..106541100hg38UCSC Ensembl
chr13:107188549..107193448hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg384900
hg194900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6484314
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177192
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00102


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