A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1137n54



Internal ID20134561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:52256302..52258268hg38UCSC Ensembl
chr10:54016062..54018028hg19UCSC Ensembl
chr10:53686068..53688034hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg381967
hg191967
hg181967
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv550893, nsv550898, nsv550884, nsv550895, nsv550896, nsv550892, nsv550885
Samples
Known GenesPRKG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1137n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss227
Observed Complex0
Frequencyn/a


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