A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17845284



Internal ID22028927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:29526623..29526623hg38UCSC Ensembl
chr1:29853135..29853135hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6241388
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17845284
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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