A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575222



Internal ID20948293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66503152..66503854hg38UCSC Ensembl
chr8:67415387..67416089hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg38703
hg19703
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278487
Samples
Known GenesC8orf46
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575222
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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