A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5437654



Internal ID216238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150613699..150613767hg38UCSC Ensembl
chr3:150331486..150331554hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16940540
Samples
Known GenesSELT
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5437654
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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