A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17841611



Internal ID22025254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4406412..4406412hg38UCSC Ensembl
chr10:4448604..4448604hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6240332
Supporting Variants
Samples
Known GenesLINC00703
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17841611
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