A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4737716



Internal ID20513678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:154583447..154583565hg38UCSC Ensembl
chr5:153963007..153963125hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275773
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4737716
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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