A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17853655



Internal ID22037298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:28444828..28444828hg38UCSC Ensembl
chr4:28446450..28446450hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38226
hg19226
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6243894
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17853655
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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