A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16960745



Internal ID41139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:190106436..190112724hg38UCSC Ensembl
chr4:191027591..191033879hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg386289
hg196289
Variant TypeCNV mobile element deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147208
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16960745
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.28926


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