A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739893



Internal ID20515868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:125028146..125028472hg38UCSC Ensembl
chr5:124363839..124364165hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270491
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739893
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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