A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv41n21



Internal ID20131762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:51308844..51311193hg38UCSC Ensembl
chr10:53068604..53070953hg19UCSC Ensembl
chr10:52738610..52740959hg18UCSC Ensembl
chr10:52738610..52740959hg17UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg382350
hg192350
hg182350
hg172350
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv523520, nsv519180
Samples
Known GenesPRKG1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv41n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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