A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053199



Internal ID19142418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:27910191..27954661hg38UCSC Ensembl
Innerchr11:27931738..27976208hg19UCSC Ensembl
Innerchr11:27888314..27932784hg18UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3844471
hg1944471
hg1844471
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3521632
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)nsv1053199
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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