A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3209408



Internal ID22357493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:52289772..52290007hg38UCSC Ensembl
chr19:52793025..52793260hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38236
hg19236
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14448058
SamplesHG00733
Known GenesZNF766
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3209408
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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