A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044636



Internal ID19133855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:25612037..25742646hg38UCSC Ensembl
Innerchr11:25633583..25764193hg19UCSC Ensembl
Innerchr11:25590159..25720769hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38130610
hg19130611
hg18130611
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3516320
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)nsv1044636
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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