A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179149



Internal ID20746189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66299426..66303994hg38UCSC Ensembl
chr15:66591764..66596332hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg384569
hg194569
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6512379
Supporting Variants
Samples
Known GenesDIS3L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179149
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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