A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016766



Internal ID19105983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:260364..343493hg38UCSC Ensembl
Innerchr6:260364..343493hg19UCSC Ensembl
Innerchr6:205364..288493hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3883130
hg1983130
hg1883130
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5874n100
Supporting Variantsnssv3652745, nssv3652746
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)nsv1016766
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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