A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv177n152



Internal ID22815880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32986772..32988365hg38UCSC Ensembl
chr1:33452373..33453966hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg381594
hg191594
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3174450, nsv3172887, nsv3170632
SamplesNA19240, HG00733, 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)dgv177n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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