A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516359



Internal ID15443652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:165463943..165487636hg38UCSC Ensembl
Innerchr6:165877431..165901124hg19UCSC Ensembl
Innerchr6:165797421..165821114hg18UCSC Ensembl
Innerchr6:165847842..165871535hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3823694
hg1923694
hg1823694
hg1723694
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv399n21
Supporting Variantsnssv661453, nssv705922, nssv667759
Samples
Known GenesPDE10A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516359
Frequency
Sample Size2026
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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