A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177756



Internal ID20744796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:81258082..81334893hg38UCSC Ensembl
chr15:81550423..81627234hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3876812
hg1976812
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496226
Supporting Variants
Samples
Known GenesIL16, STARD5, TMC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177756
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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