A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503799



Internal ID20877055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89676601..89737100hg38UCSC Ensembl
chr15:90219832..90280331hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3860500
hg1960500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026898
Samples
Known GenesPEX11A, PLIN1, WDR93
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503799
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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