A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16968183



Internal ID46102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:61907877..61908031hg38UCSC Ensembl
chr5:61203704..61203858hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5468487
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16968183
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001873


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