A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016712



Internal ID21926055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:90556334..90592094hg38UCSC Ensembl
chr7:90185648..90221408hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3835761
hg1935761
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559419
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016712
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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