A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17846259



Internal ID22029902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:50382073..50382073hg38UCSC Ensembl
chr13:50956209..50956209hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6249049
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17846259
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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