A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051760



Internal ID19140979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:119899472..119918974hg38UCSC Ensembl
Innerchr11:119770181..119789683hg19UCSC Ensembl
Innerchr11:119275391..119294893hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3819503
hg1919503
hg1819503
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1285n100
Supporting Variantsnssv3510608, nssv3507406, nssv3515273, nssv3514809
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051760
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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