A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761111



Internal ID20536971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:139209463..139209463hg38UCSC Ensembl
chr5:138545152..138545152hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16269369
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761111
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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