A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1047574



Internal ID15900760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:298700..361547hg38UCSC Ensembl
Innerchr6:298700..361547hg19UCSC Ensembl
Innerchr6:243700..306547hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3862848
hg1962848
hg1862848
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600766
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)nssv1047574
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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