A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6482742



Internal ID21140295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:21803850..21809975hg38UCSC Ensembl
chr13:22377989..22384114hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg386126
hg196126
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184992
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6482742
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