A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3195227



Internal ID22345439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:38308196..38308410hg38UCSC Ensembl
chr9:38308193..38308407hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38215
hg19215
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14392492
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3195227
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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