A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978790



Internal ID22753725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:57050879..57070019hg38UCSC Ensembl
chr8:57963438..57982578hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3819141
hg1919141
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444085
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978790
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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