A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3197966



Internal ID22347770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:16267227..16268358hg38UCSC Ensembl
chr12:16420161..16421292hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg381132
hg191132
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1748n152
Supporting Variantsnssv14448035
SamplesHG00733
Known GenesSLC15A5
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3197966
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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