A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169927



Internal ID21313988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:44889928..44926555hg38UCSC Ensembl
Outerchr11:44887942..44927645hg38UCSC Ensembl
Innerchr11:44911479..44948106hg19UCSC Ensembl
Outerchr11:44909493..44949196hg19UCSC Ensembl
Innerchr11:44868055..44904682hg18UCSC Ensembl
Outerchr11:44866069..44905772hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3839704
hg1939704
hg1839704
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14246054
SamplesNGO_23
Known GenesTSPAN18
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169927
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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