A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019439



Internal ID19108657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:290586..365708hg38UCSC Ensembl
Innerchr6:290586..365708hg19UCSC Ensembl
Innerchr6:235586..310708hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3875123
hg1975123
hg1875123
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5889n100
Supporting Variantsnssv3653689
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)nsv1019439
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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