A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1138n54



Internal ID20134562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:52256302..52258532hg38UCSC Ensembl
chr10:54016062..54018292hg19UCSC Ensembl
chr10:53686068..53688298hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg382231
hg192231
hg182231
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv550894, nsv550887, nsv550886
Samples
Known GenesPRKG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1138n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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