A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv29n54



Internal ID20133453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:1341030..1351747hg38UCSC Ensembl
chr1:1276410..1287127hg19UCSC Ensembl
chr1:1266273..1276990hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3810718
hg1910718
hg1810718
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv544988, nsv544990, nsv544989, nsv544983, nsv544982, nsv544987
Samples
Known GenesDVL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv29n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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