A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027450



Internal ID19116669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:302294..375759hg38UCSC Ensembl
Innerchr6:302294..375759hg19UCSC Ensembl
Innerchr6:247294..320759hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3873466
hg1973466
hg1873466
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5892n100
Supporting Variantsnssv3653737, nssv3653738
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)nsv1027450
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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