A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5993934



Internal ID21903277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:7506064..7759014hg38UCSC Ensembl
chr3:7547751..7800701hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38252951
hg19252951
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17532470
Samples
Known GenesGRM7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5993934
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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