A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183281



Internal ID20750321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41410212..41412237hg38UCSC Ensembl
chr15:41702410..41704435hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg382026
hg192026
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501991
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183281
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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