A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026569



Internal ID20593609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72135338..72138501hg38UCSC Ensembl
chr15:72427679..72430842hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg383164
hg193164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6515013
Supporting Variants
Samples
Known GenesSENP8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18026569
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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