A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16979663



Internal ID53820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13335492..13336920hg38UCSC Ensembl
chr6:13335724..13337152hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg381429
hg191429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5462118
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16979663
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.004685


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