A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3192203



Internal ID22342816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:92491978..92492133hg38UCSC Ensembl
chr12:92885754..92885909hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14443624
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)nsv3192203
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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