A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055057



Internal ID19144276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:80256492..80270531hg38UCSC Ensembl
Innerchr11:79967536..79981575hg19UCSC Ensembl
Innerchr11:79645184..79659223hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3814040
hg1914040
hg1814040
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1236n100
Supporting Variantsnssv3520436, nssv3520963
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)nsv1055057
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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