A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046928



Internal ID18789459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11881285..11943273hg38UCSC Ensembl
Innerchr11:11902832..11964820hg19UCSC Ensembl
Innerchr11:11859408..11921396hg18UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3861989
hg1961989
hg1861989
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1058n100
Supporting Variantsnssv3510497
Samples
Known GenesUSP47
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046928
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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