A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17854741



Internal ID22038384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:157590514..157590514hg38UCSC Ensembl
chr4:158511666..158511666hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6255576
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17854741
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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