A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17849272



Internal ID22032915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:5118994..5118994hg38UCSC Ensembl
chr18:5118993..5118993hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6259171
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17849272
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