A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026847



Internal ID18769378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:176684..395798hg38UCSC Ensembl
Innerchr6:176684..395798hg19UCSC Ensembl
Innerchr6:121684..340798hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38219115
hg19219115
hg18219115
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5869n100
Supporting Variantsnssv3650370
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)nsv1026847
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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