A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18098724



Internal ID20665764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:171856041..171856710hg38UCSC Ensembl
chr3:171573831..171574500hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38670
hg19670
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367961
Supporting Variants
Samples
Known GenesTMEM212
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18098724
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00021


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