A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016125



Internal ID21925468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:120078331..120268795hg38UCSC Ensembl
chr7:119718385..119908849hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg38190465
hg19190465
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17574361
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016125
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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