A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1047585



Internal ID15900771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:349166..378970hg38UCSC Ensembl
Innerchr6:349166..378970hg19UCSC Ensembl
Innerchr6:294166..323970hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3829805
hg1929805
hg1829805
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600776
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)nssv1047585
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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