A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5434895



Internal ID213557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:43029108..43061389hg38UCSC Ensembl
chr3:43070600..43102881hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3832282
hg1932282
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16931947
Samples
Known GenesFAM198A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5434895
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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