A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18023379



Internal ID20590419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35319819..35419786hg38UCSC Ensembl
chr15:35612020..35711987hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3899968
hg1999968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502027
Supporting Variants
Samples
Known GenesDPH6, MIR3942
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18023379
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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