A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3227304



Internal ID22369839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63833331..63833893hg38UCSC Ensembl
chr11:63600803..63601365hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38563
hg19563
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14359803
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3227304
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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