A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17853321



Internal ID22036964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:27369570..27369570hg38UCSC Ensembl
chr3:27411061..27411061hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6253857
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17853321
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