A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18012871



Internal ID20579911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:71352786..71355383hg38UCSC Ensembl
chr13:71926918..71929515hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg382598
hg192598
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6490524
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18012871
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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