A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16945220



Internal ID30812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15278916..15284458hg38UCSC Ensembl
chr4:15280540..15286082hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg385543
hg195543
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6140358
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16945220
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.10252


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer