A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026897



Internal ID20593937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89676529..89694507hg38UCSC Ensembl
chr15:90219760..90237738hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3817979
hg1917979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6497938
Supporting Variants
Samples
Known GenesPEX11A, PLIN1, WDR93
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18026897
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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