A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019033



Internal ID19108250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:302294..379003hg38UCSC Ensembl
Innerchr6:302294..379003hg19UCSC Ensembl
Innerchr6:247294..324003hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3876710
hg1976710
hg1876710
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5892n100
Supporting Variantsnssv3653749, nssv3653760, nssv3653748, nssv3747842, nssv3747841, nssv3653745, nssv3653756, nssv3653754, nssv3747843, nssv3747840, nssv3653753, nssv3747835, nssv3653750, nssv3747844, nssv3653746, nssv3653761, nssv3653759, nssv3653751, nssv3747837, nssv3747836, nssv3747838, nssv3653752, nssv3653747, nssv3653744, nssv3747839, nssv3653755, nssv3653758, nssv3653757
Samples
Known GenesDUSP22
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019033
Frequency
Sample Size11257
Observed Gain28
Observed Loss0
Observed Complex0
Frequencyn/a


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