A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17355529



Internal ID22581198
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 StatusS
Merged Variantsnsv5972887
Supporting Variants
Samples
Known GenesABI1, LINC00202-1, LINC00202-2, PDSS1
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17355529
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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