A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016679



Internal ID19105896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:264744..328345hg38UCSC Ensembl
Innerchr6:264744..328345hg19UCSC Ensembl
Innerchr6:209744..273345hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3863602
hg1963602
hg1863602
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5885n100
Supporting Variantsnssv3653558, nssv3653559
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)nsv1016679
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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