A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17359795



Internal ID22585464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:102504399..102581858hg38UCSC Ensembl
chr1:102969955..103047414hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3877460
hg1977460
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5978985
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17359795
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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