A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3192694



Internal ID22343241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12061193..12061316hg38UCSC Ensembl
chr16:12155050..12155173hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14418405
SamplesHG00514
Known GenesSNX29
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3192694
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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