A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054489



Internal ID19143708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:88702571..88762782hg38UCSC Ensembl
Innerchr11:88435739..88495950hg19UCSC Ensembl
Innerchr11:88075387..88135598hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3860212
hg1960212
hg1860212
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3522184
Samples
Known GenesGRM5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054489
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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