A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16945251



Internal ID30836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15783669..15783743hg38UCSC Ensembl
chr4:15785292..15785366hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5453396
Supporting Variants
Samples
Known GenesCD38
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16945251
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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