A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18011569



Internal ID20578609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:66003905..66013644hg38UCSC Ensembl
chr13:66578037..66587776hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg389740
hg199740
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6489071
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18011569
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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