A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5993030



Internal ID21902373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:197786394..197880237hg38UCSC Ensembl
chr3:197513265..197607108hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3893844
hg1993844
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17552116
Samples
Known GenesLRCH3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5993030
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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