A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434066



Internal ID21396068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:54207143..54207705hg38UCSC Ensembl
chr3:54241170..54241732hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg38563
hg19563
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15747674
SamplesNB07
Known GenesCACNA2D3
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434066
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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