A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5466652



Internal ID244484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169055827..169059304hg38UCSC Ensembl
chr4:169976978..169980455hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg383478
hg193478
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16959111
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5466652
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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