A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490226



Internal ID21147779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:57391631..57428704hg38UCSC Ensembl
chr13:57965765..58002838hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3837074
hg1937074
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182519
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490226
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