A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023196



Internal ID19112413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:350190..384546hg38UCSC Ensembl
Innerchr6:350190..384546hg19UCSC Ensembl
Innerchr6:295190..329546hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3834357
hg1934357
hg1834357
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5902n100
Supporting Variantsnssv3654659
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)nsv1023196
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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