A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv625666



Internal ID15849199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:24325399..24327273hg38UCSC Ensembl
Outerchr6:24323630..24330012hg38UCSC Ensembl
Innerchr6:24325627..24327501hg19UCSC Ensembl
Outerchr6:24323858..24330240hg19UCSC Ensembl
Innerchr6:24433606..24435480hg18UCSC Ensembl
Outerchr6:24431837..24438219hg18UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg386383
hg196383
hg186383
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511339
Supporting Variants
Samples1
Known GenesDCDC2
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv625666
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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