A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4758467



Internal ID20534327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61984633..61984633hg38UCSC Ensembl
chr8:62897192..62897192hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg382616
hg192616
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16296045
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4758467
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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