A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17839061



Internal ID22022704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168182878..168182878hg38UCSC Ensembl
chr1:168152116..168152116hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6245574
Supporting Variants
Samples
Known GenesTIPRL
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17839061
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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