A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054113



Internal ID18796644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11828552..11953953hg38UCSC Ensembl
Innerchr11:11850099..11975500hg19UCSC Ensembl
Innerchr11:11806675..11932076hg18UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg38125402
hg19125402
hg18125402
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3516518
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)nsv1054113
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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