A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475792



Internal ID21133345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:68124937..68184728hg38UCSC Ensembl
chr13:68699069..68758860hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3859792
hg1959792
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179619
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475792
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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