A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735441



Internal ID20511383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:128711455..128713927hg38UCSC Ensembl
chr3:128430298..128432770hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg382473
hg192473
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276522
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735441
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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