A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv26n54



Internal ID20133450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:1321172..1351426hg38UCSC Ensembl
chr1:1256552..1286806hg19UCSC Ensembl
chr1:1246415..1276669hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3830255
hg1930255
hg1830255
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv544973, nsv544974, nsv544976, nsv544975
Samples
Known GenesCPSF3L, DVL1, GLTPD1, MIR6808, TAS1R3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv26n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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