A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17855408



Internal ID22039051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25921864..25921864hg38UCSC Ensembl
chr4:25923486..25923486hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6243872
Supporting Variants
Samples
Known GenesSMIM20
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17855408
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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