A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18013131



Internal ID20580171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:76328790..76329237hg38UCSC Ensembl
chr13:76902926..76903373hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg38448
hg19448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6491650
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18013131
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00086


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