A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020198



Internal ID19109417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:279695..373441hg38UCSC Ensembl
Innerchr6:279695..373441hg19UCSC Ensembl
Innerchr6:224695..318441hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3893747
hg1993747
hg1893747
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5888n100
Supporting Variantsnssv3653666
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)nsv1020198
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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