A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16293211



Internal ID20502429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88992045..88992045hg38UCSC Ensembl
chr6:89701764..89701764hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4758231
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16293211
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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