A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169627



Internal ID21313438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:99571072..99651153hg38UCSC Ensembl
Outerchr11:99566340..99653393hg38UCSC Ensembl
Innerchr11:99441803..99521884hg19UCSC Ensembl
Outerchr11:99437071..99524124hg19UCSC Ensembl
Innerchr11:98947013..99027094hg18UCSC Ensembl
Outerchr11:98942281..99029334hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3887054
hg1987054
hg1887054
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14246032
SamplesNGO_24
Known GenesCNTN5
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169627
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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