A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490684



Internal ID21148237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:62250632..62834244hg38UCSC Ensembl
chr13:62824765..63408377hg19UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38583613
hg19583613
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192701
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490684
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer