A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041466



Internal ID19130685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:42262915..42306477hg38UCSC Ensembl
Innerchr11:42284465..42328027hg19UCSC Ensembl
Innerchr11:42241041..42284603hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3843563
hg1943563
hg1843563
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1107n100
Supporting Variantsnssv3513078
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041466
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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