A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026912



Internal ID20593952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89908403..89909375hg38UCSC Ensembl
chr15:90451635..90452607hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38973
hg19973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6509854
Supporting Variants
Samples
Known GenesC15orf38, C15orf38-AP3S2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18026912
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00057


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