A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016082



Internal ID19105300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:267610..375759hg38UCSC Ensembl
Innerchr6:267610..375759hg19UCSC Ensembl
Innerchr6:212610..320759hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38108150
hg19108150
hg18108150
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5878n100
Supporting Variantsnssv3653637
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)nsv1016082
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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