A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038045



Internal ID19127264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97542132..97685389hg38UCSC Ensembl
Innerchr11:97413132..97556389hg19UCSC Ensembl
Innerchr11:96918342..97061599hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38143258
hg19143258
hg18143258
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3504548
Samples
Known GenesMIR7976
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038045
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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