A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17853755



Internal ID22037398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:77761183..77761183hg38UCSC Ensembl
chr4:78682337..78682337hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38263
hg19263
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6254866
Supporting Variants
Samples
Known GenesCNOT6L
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17853755
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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