A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5434922



Internal ID213583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:148249661..148251188hg38UCSC Ensembl
chr3:147967448..147968975hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg381528
hg191528
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16941153
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5434922
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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