A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv402n21



Internal ID20132123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:5768328..5888325hg38UCSC Ensembl
chr7:5807959..5927956hg19UCSC Ensembl
chr7:5774485..5894482hg18UCSC Ensembl
chr7:5581200..5701197hg17UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38119998
hg19119998
hg18119998
hg17119998
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv521589, nsv521919
Samples
Known GenesOCM, RNF216, ZNF815P
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv402n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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