A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5464901



Internal ID242772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:152544885..152682495hg38UCSC Ensembl
chr4:153466037..153603647hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38137611
hg19137611
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16957067
Samples
Known GenesTMEM154
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5464901
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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