A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978889



Internal ID22753824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:131776997..131777077hg38UCSC Ensembl
chr8:132789244..132789324hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17432070
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978889
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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