A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512036



Internal ID15504775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:25208964..25213388hg38UCSC Ensembl
Outerchr8:25066480..25070904hg19UCSC Ensembl
Outerchr8:25122397..25126821hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg384425
hg194425
hg184425
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624585
Samples1
Known GenesDOCK5
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv512036
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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