A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022334



Internal ID18764868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:231934..395798hg38UCSC Ensembl
Innerchr6:231934..395798hg19UCSC Ensembl
Innerchr6:176934..340798hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38163865
hg19163865
hg18163865
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5872n100
Supporting Variantsnssv3650378
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)nsv1022334
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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