A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16981720



Internal ID55169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:45653920..45653971hg38UCSC Ensembl
chr6:45621657..45621708hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5413433
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16981720
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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