A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16979149



Internal ID53479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14734015..14734379hg38UCSC Ensembl
chr6:14734246..14734610hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38365
hg19365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5464906
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16979149
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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