A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212824



Internal ID20779864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:179474239..179522704hg38UCSC Ensembl
chr4:180395393..180443857hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3848466
hg1948465
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6375973
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212824
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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