A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048988



Internal ID19138207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:23318239..23497509hg38UCSC Ensembl
Innerchr11:23339785..23519055hg19UCSC Ensembl
Innerchr11:23296361..23475631hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38179271
hg19179271
hg18179271
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3519784
Samples
Known GenesMIR8054
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048988
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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