A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3227565



Internal ID22370015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:16555256..16638155hg38UCSC Ensembl
Outerchr9:16555254..16638153hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3882900
hg1982900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14282840
SamplesHG00513
Known GenesBNC2
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3227565
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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