A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv624816



Internal ID15501666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:132069522..132071473hg38UCSC Ensembl
Outerchr11:131939416..131941367hg19UCSC Ensembl
Outerchr11:131444626..131446577hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg381952
hg191952
hg181952
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512244
Supporting Variants
Samples1
Known GenesNTM
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv624816
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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