A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18101433



Internal ID20668473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:48370501..48380200hg38UCSC Ensembl
chr3:48411991..48421690hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg389700
hg199700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6368296
Supporting Variants
Samples
Known GenesFBXW12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18101433
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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