A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733794



Internal ID20509725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:163574156..163574227hg38UCSC Ensembl
chr5:163001162..163001233hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16277127
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733794
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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