A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16961244



Internal ID41468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:182889524..182889706hg38UCSC Ensembl
chr4:183810677..183810859hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5471651
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16961244
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.005776


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