A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970827



Internal ID22745762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:70033303..70049084hg38UCSC Ensembl
chr8:70945538..70961319hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3815782
hg1915782
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17443581
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970827
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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