A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761977



Internal ID20537837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:78358344..78358344hg38UCSC Ensembl
chr5:77654168..77654168hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16281458
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761977
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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