A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189587



Internal ID20756627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101388760..101647699hg38UCSC Ensembl
chr15:101928965..102187902hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38258940
hg19258938
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6507902
Supporting Variants
Samples
Known GenesPCSK6, TM2D3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189587
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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