A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18079834



Internal ID20646874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:158128799..158129697hg38UCSC Ensembl
chr2:158985311..158986209hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg38899
hg19899
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6349258
Supporting Variants
Samples
Known GenesUPP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18079834
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00276


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