A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039866



Internal ID19129085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:12017654..12033646hg38UCSC Ensembl
Innerchr11:12039201..12055193hg19UCSC Ensembl
Innerchr11:11995777..12011769hg18UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3815993
hg1915993
hg1815993
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3509618
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)nsv1039866
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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