A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6086989



Internal ID21996222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:69086486..69086486hg38UCSC Ensembl
chr17:67082627..67082627hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17621469
Samples
Known GenesABCA6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6086989
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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