A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045989



Internal ID18788520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67744858..67882157hg38UCSC Ensembl
Innerchr11:67512329..67649628hg19UCSC Ensembl
Innerchr11:67268905..67406204hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38137300
hg19137300
hg18137300
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1217n100
Supporting Variantsnssv3710634
Samples
Known GenesFAM86C2P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045989
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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