A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033119



Internal ID19122341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:260364..379003hg38UCSC Ensembl
Innerchr6:260364..379003hg19UCSC Ensembl
Innerchr6:205364..324003hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38118640
hg19118640
hg18118640
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5880n100
Supporting Variantsnssv3747764, nssv3652754, nssv3747763
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)nsv1033119
Frequency
Sample Size11257
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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