A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511927



Internal ID15851352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:168316482..168318268hg38UCSC Ensembl
Outerchr6:168717162..168718948hg19UCSC Ensembl
Outerchr6:168460011..168461797hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381787
hg191787
hg181787
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624464
Samples1
Known GenesDACT2
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511927
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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