A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053189



Internal ID18795720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4101889..4337814hg38UCSC Ensembl
Innerchr11:4123119..4359044hg19UCSC Ensembl
Innerchr11:4079695..4315620hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38235926
hg19235926
hg18235926
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3706398
Samples
Known GenesLOC100506082, RRM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053189
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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