A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202186



Internal ID22351386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:10238658..10238721hg38UCSC Ensembl
chr12:10391257..10391320hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14441779
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3202186
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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