A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17839258



Internal ID22022901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23372458..23372458hg38UCSC Ensembl
chr1:23698951..23698951hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6257487
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17839258
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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