A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018642



Internal ID19107859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:249798..361143hg38UCSC Ensembl
Innerchr6:249798..361143hg19UCSC Ensembl
Innerchr6:194798..306143hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38111346
hg19111346
hg18111346
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5874n100
Supporting Variantsnssv3650389
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)nsv1018642
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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