A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035017



Internal ID21944360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67927582..67964131hg38UCSC Ensembl
chr16:67961485..67998034hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3836550
hg1936550
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17634545
Samples
Known GenesCTRL, LCAT, PSKH1, PSMB10, SLC12A4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035017
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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