A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040312



Internal ID19129531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:106428632..106466395hg38UCSC Ensembl
Innerchr11:106299359..106337122hg19UCSC Ensembl
Innerchr11:105804569..105842332hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3837764
hg1937764
hg1837764
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3507171
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)nsv1040312
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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