A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760997



Internal ID20536857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:190856233..190856233hg38UCSC Ensembl
chr3:190574022..190574022hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289523
Samples
Known GenesGMNC
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760997
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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