A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488533



Internal ID21146086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:39309700..39328509hg38UCSC Ensembl
chr13:39883837..39902646hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3818810
hg1918810
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179313
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488533
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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