A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv405n21



Internal ID22766597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:11158566..11436192hg38UCSC Ensembl
chr7:11198193..11475819hg19UCSC Ensembl
chr7:11164718..11442344hg18UCSC Ensembl
chr7:10971433..11249059hg17UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38277627
hg19277627
hg18277627
hg17277627
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv523279, nsv518180
Samples
Known GenesPHF14, THSD7A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv405n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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