A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053989



Internal ID19143208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:81275309..81306208hg38UCSC Ensembl
Innerchr11:80986352..81017251hg19UCSC Ensembl
Innerchr11:80664000..80694899hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3830900
hg1930900
hg1830900
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1241n100
Supporting Variantsnssv3515288
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)nsv1053989
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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