A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045993



Internal ID19135212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55587591..55636296hg38UCSC Ensembl
Innerchr11:55355067..55403772hg19UCSC Ensembl
Innerchr11:55111643..55160348hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3848706
hg1948706
hg1848706
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1174n100
Supporting Variantsnssv3517642
Samples
Known GenesOR4C11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045993
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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