A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3196636



Internal ID22346615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:108578642..108583182hg38UCSC Ensembl
chr12:108972418..108976958hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg384541
hg194541
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1986n152
Supporting Variantsnssv14444003
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)nsv3196636
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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