A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010101



Internal ID21919444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:106724916..106731743hg38UCSC Ensembl
chr8:107737144..107743971hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg386828
hg196828
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578082
Samples
Known GenesOXR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010101
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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