A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191352



Internal ID20758393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:103417396..103443424hg38UCSC Ensembl
chr13:104069746..104095774hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3826029
hg1926029
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6492617
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191352
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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