A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17854703



Internal ID22038346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:153348711..153348711hg38UCSC Ensembl
chr4:154269863..154269863hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6255538
Supporting Variants
Samples
Known GenesMND1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17854703
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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