A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555276



Internal ID15995999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67734155..67947557hg38UCSC Ensembl
Innerchr11:67501626..67715028hg19UCSC Ensembl
Innerchr11:67258202..67471604hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38213403
hg19213403
hg18213403
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174815
SamplesHGDP00697
Known GenesFAM86C2P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555276
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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