A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17411918



Internal ID22469788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:116668944..116669552hg38UCSC Ensembl
chr6:116990107..116990715hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38609
hg19609
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5905958
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17411918
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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