A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980368



Internal ID22755303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119543916..119630994hg38UCSC Ensembl
chr10:121303428..121390506hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3887079
hg1987079
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17350023
Samples
Known GenesTIAL1
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5980368
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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