A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6934n152



Internal ID22822637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165081465..165083903hg38UCSC Ensembl
chr4:166002617..166005055hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg382439
hg192439
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3188203, nsv3173701
SamplesNA19240, HG00733, HG00514
Known GenesTMEM192
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv6934n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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