A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975276



Internal ID22750211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:12344905..12755014hg38UCSC Ensembl
chr20:12325553..12735661hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38410110
hg19410109
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17399679
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975276
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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