A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17845300



Internal ID22028943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:71160551..71160551hg38UCSC Ensembl
chr13:71734683..71734683hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6249270
Supporting Variants
Samples
Known GenesLINC00348
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17845300
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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