A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4768016



Internal ID20543876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:26680341..26680341hg38UCSC Ensembl
chr8:26537858..26537858hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38194
hg19194
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16296434
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4768016
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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