A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511855



Internal ID15851280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:21850375..21853154hg38UCSC Ensembl
Outerchr6:21850606..21853385hg19UCSC Ensembl
Outerchr6:21958585..21961364hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg382780
hg192780
hg182780
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624385
Samples1
Known GenesCASC15
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511855
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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