A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019993



Internal ID19109212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:271761..384097hg38UCSC Ensembl
Innerchr6:271761..384097hg19UCSC Ensembl
Innerchr6:216761..329097hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38112337
hg19112337
hg18112337
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5878n100
Supporting Variantsnssv3653661
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)nsv1019993
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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