A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17842332



Internal ID22025975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:212558828..212558828hg38UCSC Ensembl
chr1:212732170..212732170hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6258120
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17842332
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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