A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5994713



Internal ID21904056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:78758303..78760361hg38UCSC Ensembl
chr3:78807453..78809511hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg382059
hg192059
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17541670
Samples
Known GenesROBO1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5994713
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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