A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv469n152



Internal ID22816172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:175231430..175232801hg38UCSC Ensembl
chr1:175200566..175201937hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg381372
hg191372
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3545594, nsv3553061
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
Single strand sequencing, and assortment analysis
PlatformIllumina HiSeq
Strand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv469n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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