A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4100n152



Internal ID22819803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:5144451..5144526hg38UCSC Ensembl
chr19:5144462..5144537hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3190532, nsv3190570
SamplesNA19240, HG00733, HG00514
Known GenesKDM4B
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv4100n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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