A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017293



Internal ID19106510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:260364..351364hg38UCSC Ensembl
Innerchr6:260364..351364hg19UCSC Ensembl
Innerchr6:205364..296364hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3891001
hg1991001
hg1891001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5874n100
Supporting Variantsnssv3747762
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)nsv1017293
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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