A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555323



Internal ID16342732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:69595537..69615426hg38UCSC Ensembl
Innerchr11:69410305..69430194hg19UCSC Ensembl
Innerchr11:69119486..69139375hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3819890
hg1919890
hg1819890
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1991n54
Supporting Variantsnssv1174821
SamplesHGDP00878
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555323
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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