A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17855161



Internal ID22038804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:68261064..68261064hg38UCSC Ensembl
chr4:69126782..69126782hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6244197
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17855161
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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