A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv41n54



Internal ID20133465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:1713469..1740343hg38UCSC Ensembl
chr1:1644908..1671782hg19UCSC Ensembl
chr1:1634768..1661642hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3826875
hg1926875
hg1826875
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv545035, nsv545036
Samples
Known GenesCDK11A, CDK11B, SLC35E2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv41n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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