A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3518018



Internal ID18816299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54554865..54586670hg38UCSC Ensembl
Innerchr11:51532610..51564415hg19UCSC Ensembl
Innerchr11:51389186..51420991hg18UCSC Ensembl
Cytoband11p11.11
Allele length
AssemblyAllele length
hg3831806
hg1931806
hg1831806
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036089
Supporting Variants
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)nssv3518018
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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