A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053433



Internal ID19142652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:78917219..79051582hg38UCSC Ensembl
Innerchr11:78628264..78762627hg19UCSC Ensembl
Innerchr11:78305912..78440275hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38134364
hg19134364
hg18134364
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3522467
Samples
Known GenesTENM4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053433
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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