A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4750886



Internal ID20526746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:63988614..63988614hg38UCSC Ensembl
chr8:64901171..64901171hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266110
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4750886
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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