A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026911



Internal ID20593951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89905274..89914276hg38UCSC Ensembl
chr15:90448506..90457508hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg389003
hg199003
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6508435
Supporting Variants
Samples
Known GenesC15orf38, C15orf38-AP3S2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18026911
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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