A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16981306



Internal ID54911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36158730..36158790hg38UCSC Ensembl
chr6:36126507..36126567hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5471707
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16981306
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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