A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4747326



Internal ID20523344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:116862685..116891112hg38UCSC Ensembl
chr5:116198381..116226808hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3828428
hg1928428
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16267023
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4747326
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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