A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571778



Internal ID20944849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:103384252..103415352hg38UCSC Ensembl
chr8:104396480..104427580hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3831101
hg1931101
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276309
Samples
Known GenesDCAF13, SLC25A32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571778
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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