A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049615



Internal ID19138834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:81154316..81167962hg38UCSC Ensembl
Innerchr11:80865359..80879005hg19UCSC Ensembl
Innerchr11:80543007..80556653hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3813647
hg1913647
hg1813647
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3512084
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)nsv1049615
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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