A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6022587



Internal ID21931930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:69078029..69080464hg38UCSC Ensembl
chr17:67074170..67076605hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg382436
hg192436
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622300
Samples
Known GenesABCA6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6022587
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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