A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483425



Internal ID21140978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:104343078..104817307hg38UCSC Ensembl
chr13:104995428..105469658hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg38474230
hg19474231
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180319
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483425
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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