A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3195993



Internal ID22346086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35527213..35527427hg38UCSC Ensembl
chr19:36018115..36018329hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38215
hg19215
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14420485
SamplesHG00514
Known GenesSBSN
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3195993
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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