A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178511



Internal ID20745551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:46836936..46869464hg38UCSC Ensembl
chr15:47129134..47161662hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3832529
hg1932529
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500176
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178511
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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