A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210212



Internal ID20777252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:120917301..120925600hg38UCSC Ensembl
chr4:121838456..121846755hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg388300
hg198300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6382064
Supporting Variants
Samples
Known GenesPRDM5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210212
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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