A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4731748



Internal ID20507669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87073919..87074010hg38UCSC Ensembl
chr5:86369736..86369827hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16283826
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4731748
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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