A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267274



Internal ID20476492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79165948..79165948hg38UCSC Ensembl
chr10:80925705..80925705hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4766901
Supporting Variants
Samples
Known GenesZMIZ1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267274
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