A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555253



Internal ID15995976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67265605..67397024hg38UCSC Ensembl
Innerchr11:67033076..67164495hg19UCSC Ensembl
Innerchr11:66789652..66921071hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38131420
hg19131420
hg18131420
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174659
Samples1798860210_A
Known GenesADRBK1, ANKRD13D, CLCF1, LOC100130987, POLD4, RAD9A, SSH3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555253
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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