A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193158



Internal ID20760198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51721031..51730778hg38UCSC Ensembl
chr15:52013228..52022975hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg389748
hg199748
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500722
Supporting Variants
Samples
Known GenesLYSMD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193158
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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