A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028946



Internal ID18771478
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 StatusM
Merged Variants
Supporting Variantsnssv3654638
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)nsv1028946
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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