A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553948



Internal ID15994671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:30811679..30905653hg38UCSC Ensembl
Innerchr11:30833226..30927200hg19UCSC Ensembl
Innerchr11:30789802..30883776hg18UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3893975
hg1993975
hg1893975
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv770673
Samples
Known GenesDCDC5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553948
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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