A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1047569



Internal ID15900755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:283619..390105hg38UCSC Ensembl
Innerchr6:283619..390105hg19UCSC Ensembl
Innerchr6:228619..335105hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38106487
hg19106487
hg18106487
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600760
Supporting Variants
Samples
Known GenesDUSP22
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1047569
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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