A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5446458



Internal ID224780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2494078..2494852hg38UCSC Ensembl
chr4:2495805..2496579hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38775
hg19775
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16947536
Samples
Known GenesRNF4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5446458
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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