A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv328n152



Internal ID22816031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:93876120..93878626hg38UCSC Ensembl
chr1:94341676..94344182hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg382507
hg192507
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3175292, nsv3175540, nsv3181384
SamplesNA19240, HG00733, HG00514
Known GenesDNTTIP2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv328n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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