A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019309



Internal ID19108527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:271761..382897hg38UCSC Ensembl
Innerchr6:271761..382897hg19UCSC Ensembl
Innerchr6:216761..327897hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38111137
hg19111137
hg18111137
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5878n100
Supporting Variantsnssv3653660
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)nsv1019309
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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