A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017828



Internal ID19107045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:264744..384521hg38UCSC Ensembl
Innerchr6:264744..384521hg19UCSC Ensembl
Innerchr6:209744..329521hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38119778
hg19119778
hg18119778
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5878n100
Supporting Variantsnssv3653602
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)nsv1017828
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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