A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736526



Internal ID20512475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:131357283..131357508hg38UCSC Ensembl
chr3:131076127..131076352hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38226
hg19226
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16277111
Samples
Known GenesLOC339874
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736526
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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