A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763791



Internal ID20539651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:115075991..115075991hg38UCSC Ensembl
chr8:116088220..116088220hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16296662
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763791
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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