A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv403n21



Internal ID20132124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:6148152..6173025hg38UCSC Ensembl
chr7:6187783..6212656hg19UCSC Ensembl
chr7:6154309..6179181hg18UCSC Ensembl
chr7:5961024..5985896hg17UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3824874
hg1924874
hg1824873
hg1724873
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv522217, nsv527386
Samples
Known GenesCYTH3, USP42
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv403n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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