A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502518



Internal ID20875764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58429486..58438536hg38UCSC Ensembl
chr15:58721685..58730735hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg389051
hg199051
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026170
Samples
Known GenesLIPC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502518
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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