A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764973



Internal ID20540833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:122989697..122989697hg38UCSC Ensembl
chr8:124001937..124001937hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266397
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764973
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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