A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17578082



Internal ID21770125
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 StatusS
Merged Variantsnsv6010101
Supporting Variants
Samples
Known GenesOXR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17578082
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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