A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052432



Internal ID18794963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:71456403..71501961hg38UCSC Ensembl
Innerchr11:71167449..71213007hg19UCSC Ensembl
Innerchr11:70845097..70890655hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3845559
hg1945559
hg1845559
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3519995
Samples
Known GenesMIR6754, NADSYN1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052432
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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