A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026907



Internal ID20593947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89889828..89891532hg38UCSC Ensembl
chr15:90433060..90434764hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381705
hg191705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499048
Supporting Variants
Samples
Known GenesAP3S2, C15orf38-AP3S2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18026907
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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