A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040880



Internal ID18783411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:43931554..43947681hg38UCSC Ensembl
Innerchr11:43953104..43969231hg19UCSC Ensembl
Innerchr11:43909680..43925807hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3816128
hg1916128
hg1816128
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1109n100
Supporting Variantsnssv3506278
Samples
Known GenesC11orf96
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040880
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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