A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5438400



Internal ID216966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:152590627..152599618hg38UCSC Ensembl
chr3:152308416..152317407hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg388992
hg198992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16939056
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5438400
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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