A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18024566



Internal ID20591606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44564283..44566954hg38UCSC Ensembl
chr15:44856481..44859152hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg382672
hg192672
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500132
Supporting Variants
Samples
Known GenesSPG11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18024566
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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