A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037876



Internal ID19127095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:80261889..80278911hg38UCSC Ensembl
Innerchr11:79972933..79989955hg19UCSC Ensembl
Innerchr11:79650581..79667603hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3817023
hg1917023
hg1817023
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1239n100
Supporting Variantsnssv3504389
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)nsv1037876
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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