A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476148



Internal ID21133701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77026201..77027900hg38UCSC Ensembl
chr13:77600336..77602035hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177150
Samples
Known GenesFBXL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476148
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