A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17839201



Internal ID22022844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:34823048..34823048hg38UCSC Ensembl
chr8:34680566..34680566hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38222
hg19222
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6245865
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17839201
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