A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016533



Internal ID21925876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:6468473..6469400hg38UCSC Ensembl
chr7:6508104..6509031hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38928
hg19928
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559223
Samples
Known GenesKDELR2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016533
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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