A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560882



Internal ID20933953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66799829..66800327hg38UCSC Ensembl
chr8:67712064..67712562hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg38499
hg19499
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278503
Samples
Known GenesC8orf44-SGK3, SGK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560882
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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