A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736190



Internal ID20512137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177517780..177518500hg38UCSC Ensembl
chr5:176944781..176945501hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38721
hg19721
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16263401
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736190
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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