A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511327



Internal ID15850752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31269452..31270275hg38UCSC Ensembl
Outerchr6:31269284..31270332hg38UCSC Ensembl
Innerchr6:31237229..31238052hg19UCSC Ensembl
Outerchr6:31237061..31238109hg19UCSC Ensembl
Innerchr6:31345208..31346031hg18UCSC Ensembl
Outerchr6:31345040..31346088hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg381049
hg191049
hg181049
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625533
Samples1
Known GenesHLA-C
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511327
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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