A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511873



Internal ID15851298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:32655516..32660188hg38UCSC Ensembl
Outerchr6:32623293..32627965hg19UCSC Ensembl
Outerchr6:32731271..32735943hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg384673
hg194673
hg184673
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624405
Samples1
Known GenesHLA-DQB1
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511873
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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