A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5434555



Internal ID213228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:193860235..193861546hg38UCSC Ensembl
chr3:193578024..193579335hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg381312
hg191312
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16944463
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5434555
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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