A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026610



Internal ID21935953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68883495..68886480hg38UCSC Ensembl
chr17:66879636..66882621hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg382986
hg192986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636614
Samples
Known GenesABCA8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026610
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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