A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024491



Internal ID19113708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:267610..315197hg38UCSC Ensembl
Innerchr6:267610..315197hg19UCSC Ensembl
Innerchr6:212610..260197hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3847588
hg1947588
hg1847588
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5882n100
Supporting Variantsnssv3653627, nssv3653628, nssv3747797, nssv3653629
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)nsv1024491
Frequency
Sample Size11257
Observed Gain2
Observed Loss2
Observed Complex0
Frequencyn/a


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