A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17854695



Internal ID22038338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:152628601..152628601hg38UCSC Ensembl
chr4:153549753..153549753hg19UCSC 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 Variantsnsv6255530
Supporting Variants
Samples
Known GenesTMEM154
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17854695
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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