A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3190994



Internal ID22341769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:13424325..13425694hg38UCSC Ensembl
chr9:13424324..13425693hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg381370
hg191370
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9484n152
Supporting Variantsnssv14402525
SamplesNA19240
Known GenesFLJ41200
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3190994
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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