A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16947096



Internal ID32092
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 StatusS
Merged Variantsnsv5434282
Supporting Variants
Samples
Known GenesMIR4275
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16947096
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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