A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367536



Internal ID21025089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:158799915..158807861hg38UCSC Ensembl
chr3:158517704..158525650hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg387947
hg197947
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094646
Samples
Known GenesMFSD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367536
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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