A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17855342



Internal ID22038985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:17854684..17854684hg38UCSC Ensembl
chr4:17856307..17856307hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6243798
Supporting Variants
Samples
Known GenesLCORL
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17855342
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