A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5974642



Internal ID22749577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:128146719..128156170hg38UCSC Ensembl
chr10:129944983..129954434hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg389452
hg199452
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359773
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5974642
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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