A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17839288



Internal ID22022931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:170889152..170889152hg38UCSC Ensembl
chr1:170858293..170858293hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6245598
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17839288
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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