A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028605



Internal ID19117823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:349386..381137hg38UCSC Ensembl
Innerchr6:349386..381137hg19UCSC Ensembl
Innerchr6:294386..326137hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3831752
hg1931752
hg1831752
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5902n100
Supporting Variantsnssv3747895
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)nsv1028605
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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