A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17852354



Internal ID22035997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:47580234..47580234hg38UCSC Ensembl
chr1:48045906..48045906hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6243224
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17852354
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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