A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048411



Internal ID18790942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:87841324..88022773hg38UCSC Ensembl
Innerchr11:87552216..87755941hg19UCSC Ensembl
Innerchr11:87229864..87395589hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38181450
hg19203726
hg18165726
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1249n100
Supporting Variantsnssv3511976
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)nsv1048411
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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