A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553541



Internal ID15994264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11854200..11864294hg38UCSC Ensembl
Innerchr11:11875747..11885841hg19UCSC Ensembl
Innerchr11:11832323..11842417hg18UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3810095
hg1910095
hg1810095
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1656n54
Supporting Variantsnssv768243, nssv768244
Samples
Known GenesUSP47
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553541
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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