A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5434518



Internal ID213191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139466019..139466153hg38UCSC Ensembl
chr3:139184861..139184995hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17734975
Samples
Known GenesRBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5434518
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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