A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3210382



Internal ID22358307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67222092..67222610hg38UCSC Ensembl
chr11:66989563..66990081hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38519
hg19519
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14360534, nssv14360532, nssv14360533
SamplesNA19238, NA19239, NA19240
Known GenesKDM2A
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3210382
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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