A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17845977



Internal ID22029620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:106844566..106844566hg38UCSC Ensembl
chr13:107496914..107496914hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38247
hg19247
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6249585
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17845977
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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