A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733323



Internal ID20509251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:68186338..68186458hg38UCSC Ensembl
chr5:67482166..67482286hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288375
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733323
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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