A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5434383



Internal ID213061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196305721..196306339hg38UCSC Ensembl
chr3:196032592..196033210hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38619
hg19619
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16944617
Samples
Known GenesTCTEX1D2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5434383
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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