A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18013531



Internal ID20580571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:80114701..80117200hg38UCSC Ensembl
chr13:80688836..80691335hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6481596
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18013531
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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