A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18010464



Internal ID20577504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:59132017..59132373hg38UCSC Ensembl
chr13:59706151..59706507hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg38357
hg19357
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6487028
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18010464
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00959


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