A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975825



Internal ID22750760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:111428666..111428811hg38UCSC Ensembl
chr1:111971288..111971433hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17356629
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975825
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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