A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3209138



Internal ID22357257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:125856279..125856329hg38UCSC Ensembl
chr12:126340825..126340875hg19UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2041n152
Supporting Variantsnssv14386766
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)nsv3209138
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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