A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760953



Internal ID20536813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:127812256..127812256hg38UCSC Ensembl
chr8:128824502..128824502hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16279350
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760953
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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