A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733871



Internal ID20509802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:80301293..80301374hg38UCSC Ensembl
chr5:79597112..79597193hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289948
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733871
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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