A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562712



Internal ID20935783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:106605631..106606319hg38UCSC Ensembl
chr8:107617859..107618547hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38689
hg19689
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276360
Samples
Known GenesOXR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562712
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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