A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv399n21



Internal ID22766591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165463943..165495974hg38UCSC Ensembl
chr6:165877431..165909462hg19UCSC Ensembl
chr6:165797421..165829452hg18UCSC Ensembl
chr6:165847842..165879873hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3832032
hg1932032
hg1832032
hg1732032
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv528284, nsv516359
Samples
Known GenesPDE10A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv399n21
Frequency
Sample Size2026
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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