A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3222265



Internal ID22366390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133255277..133255338hg38UCSC Ensembl
chr9:136130664..136130725hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14349309
SamplesNA19238
Known GenesABO
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3222265
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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