A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4261n152



Internal ID22819964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38131783..38132758hg38UCSC Ensembl
chr19:38622423..38623398hg19UCSC Ensembl
Cytoband19q13.13
Allele length
AssemblyAllele length
hg38976
hg19976
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3198983, nsv3209610
SamplesNA19240, HG00514
Known GenesSIPA1L3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv4261n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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