A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14382566



Internal ID22288566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:43006966..43019614hg38UCSC Ensembl
chr9:42963634..42976299hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3812649
hg1912666
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3229281
Supporting Variants
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)nssv14382566
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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