A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5462641



Internal ID240565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174843863..175490971hg38UCSC Ensembl
chr4:175765014..176412122hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38647109
hg19647109
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16958456
Samples
Known GenesADAM29
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5462641
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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