A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225965



Internal ID22368935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:52731434..52732284hg38UCSC Ensembl
chr14:53198152..53199002hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38851
hg19851
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14371811, nssv14371812
SamplesNA19239, NA19240
Known GenesSTYX
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225965
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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