A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18013126



Internal ID20580166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:76255301..76256000hg38UCSC Ensembl
chr13:76829437..76830136hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6476241
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18013126
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00032


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