A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18097361



Internal ID20664401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:168575361..168575868hg38UCSC Ensembl
chr3:168293149..168293656hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38508
hg19508
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6370137
Supporting Variants
Samples
Known GenesEGFEM1P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18097361
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00117


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