A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763723



Internal ID20539583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:39958718..39958718hg38UCSC Ensembl
chr5:39958820..39958820hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg381373
hg191373
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16271901
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763723
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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