A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5434282



Internal ID212962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:28794498..28865697hg38UCSC Ensembl
chr4:28796120..28867319hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3871200
hg1971200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16947096
Samples
Known GenesMIR4275
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5434282
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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