A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5972887



Internal ID22747822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26648647..26934429hg38UCSC Ensembl
chr10:26937576..27223358hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38285783
hg19285783
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17355529
Samples
Known GenesABI1, LINC00202-1, LINC00202-2, PDSS1
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5972887
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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