A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050392



Internal ID19139611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55006405..55272314hg38UCSC Ensembl
Innerchr11:54773881..55039790hg19UCSC Ensembl
Innerchr11:54530457..54796366hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38265910
hg19265910
hg18265910
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1165n100
Supporting Variantsnssv3520848
Samples
Known GenesTRIM48
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050392
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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