A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760329



Internal ID20536189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46776159..46776159hg38UCSC Ensembl
chr1:47241831..47241831hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16290097
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760329
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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