A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486914



Internal ID21144467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:34190310..34192746hg38UCSC Ensembl
chr13:34764447..34766883hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg382437
hg192437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18008823
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486914
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer