A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6494815



Internal ID21152368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:28785036..28786724hg38UCSC Ensembl
chr13:29359173..29360861hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg381689
hg191689
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178752
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6494815
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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