A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202559



Internal ID22351706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:19096401..19096505hg38UCSC Ensembl
chr12:19249335..19249439hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14392854
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3202559
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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