A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5176n54



Internal ID22773071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:63042506..63087176hg38UCSC Ensembl
chr16:63076410..63121080hg19UCSC Ensembl
chr16:61633911..61678581hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3844671
hg1944671
hg1844671
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv572883, nsv572886, nsv572881, nsv572884
Samples1798860084_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5176n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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