A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17842195



Internal ID22025838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:198566764..198566764hg38UCSC Ensembl
chr1:198535894..198535894hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6258012
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17842195
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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