A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765831



Internal ID20541691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:41330211..41330211hg38UCSC Ensembl
chr8:41187730..41187730hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38213
hg19213
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273501
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765831
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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