A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044269



Internal ID19133488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:95169007..95229323hg38UCSC Ensembl
Innerchr11:94902171..94962487hg19UCSC Ensembl
Innerchr11:94541819..94602135hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3860317
hg1960317
hg1860317
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3514044
Samples
Known GenesSESN3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044269
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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