A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014384



Internal ID21923727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:45811034..45814311hg38UCSC Ensembl
chr7:45850633..45853910hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg383278
hg193278
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561304
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014384
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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