A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042784



Internal ID18785315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:132775265..132868558hg38UCSC Ensembl
Innerchr11:132645160..132738453hg19UCSC Ensembl
Innerchr11:132150370..132243663hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3893294
hg1993294
hg1893294
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3710768
Samples
Known GenesOPCML
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042784
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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