A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17840328



Internal ID22023971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23930414..23930414hg38UCSC Ensembl
chr1:24256904..24256904hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6257545
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17840328
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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