A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511336



Internal ID15850761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:5898178..5898490hg38UCSC Ensembl
Outerchr6:5898142..5900035hg38UCSC Ensembl
Innerchr6:5898411..5898723hg19UCSC Ensembl
Outerchr6:5898375..5900268hg19UCSC Ensembl
Innerchr6:5843410..5843722hg18UCSC Ensembl
Outerchr6:5843374..5845267hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg381894
hg191894
hg181894
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625633
Samples1
Known Genes
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511336
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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