A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3207344



Internal ID22355745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:18507465..18507519hg38UCSC Ensembl
chr16:14982363..14982417hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14446390
SamplesHG00733
Known GenesNOMO1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3207344
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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