A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015566



Internal ID21924909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:72768344..72840811hg38UCSC Ensembl
chr8:73680579..73753046hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3872468
hg1972468
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583221
Samples
Known GenesKCNB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015566
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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