A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4526n152



Internal ID22820229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:26333427..26336723hg38UCSC Ensembl
chr2:26556295..26559591hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg383297
hg193297
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3179631, nsv3180963, nsv3189790
SamplesNA19240, HG00733, HG00514
Known GenesGPR113
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv4526n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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