A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039927



Internal ID19129146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:81759499..81884472hg38UCSC Ensembl
Innerchr11:81470541..81595514hg19UCSC Ensembl
Innerchr11:81148189..81273162hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38124974
hg19124974
hg18124974
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1242n100
Supporting Variantsnssv3509685
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)nsv1039927
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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