A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434063



Internal ID21396065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:51594089..51594860hg38UCSC Ensembl
chr3:51628105..51628876hg19UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg38772
hg19772
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15749703
SamplesMDQ025
Known GenesRAD54L2
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434063
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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