A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193897



Internal ID20760938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80694001..80698100hg38UCSC Ensembl
chr15:80986342..80990441hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg384100
hg194100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6497480
Supporting Variants
Samples
Known GenesABHD17C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193897
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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