A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052132



Internal ID19141351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:80261889..80277537hg38UCSC Ensembl
Innerchr11:79972933..79988581hg19UCSC Ensembl
Innerchr11:79650581..79666229hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3815649
hg1915649
hg1815649
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1239n100
Supporting Variantsnssv3518961
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)nsv1052132
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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