A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16956046



Internal ID38001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:113209317..113222395hg38UCSC Ensembl
chr4:114130473..114143551hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3813079
hg1913079
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5463881
Supporting Variants
Samples
Known GenesANK2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16956046
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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