A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16954131



Internal ID36746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:119061381..119067400hg38UCSC Ensembl
chr4:119982536..119988555hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg386020
hg196020
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5457314
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16954131
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000475


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