A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6479464



Internal ID21137017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:47251701..47280400hg38UCSC Ensembl
chr13:47825836..47854535hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3828700
hg1928700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183160
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6479464
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