A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3654638



Internal ID18606233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:334825..404771hg38UCSC Ensembl
Innerchr6:334825..404771hg19UCSC Ensembl
Innerchr6:279825..349771hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3869947
hg1969947
hg1869947
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028946
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)nssv3654638
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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