A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18005941



Internal ID20572981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:102946671..102951191hg38UCSC Ensembl
chr13:103599021..103603541hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg384521
hg194521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6494284
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18005941
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00094


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