A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490067



Internal ID21147620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:48956001..48985400hg38UCSC Ensembl
chr13:49530137..49559536hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3829400
hg1929400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184128
Samples
Known GenesFNDC3A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490067
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