A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030962



Internal ID18773494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:302294..447036hg38UCSC Ensembl
Innerchr6:302294..447036hg19UCSC Ensembl
Innerchr6:247294..392036hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38144743
hg19144743
hg18144743
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5884n100
Supporting Variantsnssv3653824
Samples
Known GenesDUSP22, IRF4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030962
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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