A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755078



Internal ID20530938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:143182126..143182126hg38UCSC Ensembl
chr8:144263543..144263543hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38349
hg19349
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16269073
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755078
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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