A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17843995



Internal ID22027638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:97268741..97268741hg38UCSC Ensembl
chr12:97662519..97662519hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg38259
hg19259
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6248486
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17843995
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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