A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17847748



Internal ID22031391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:71729432..71729432hg38UCSC Ensembl
chr16:71763335..71763335hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6250411
Supporting Variants
Samples
Known GenesAP1G1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17847748
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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