A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1897n152



Internal ID22817600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:71795379..71796795hg38UCSC Ensembl
chr12:72189159..72190575hg19UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg381417
hg191417
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3200161, nsv3204808
SamplesHG00733, HG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv1897n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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