A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3650378



Internal ID18601973
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 StatusS
Merged Variantsnsv1022334
Supporting Variants
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)nssv3650378
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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