A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3196575



Internal ID22346560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67712970..67720634hg38UCSC Ensembl
chr16:67746873..67754537hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg387665
hg197665
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14387391
SamplesNA19240
Known GenesGFOD2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3196575
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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