A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17855943



Internal ID22039586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:103788455..103788455hg38UCSC Ensembl
chr4:104709612..104709612hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38209
hg19209
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6255079
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17855943
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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