A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1503n54



Internal ID22769398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133761946..133776587hg38UCSC Ensembl
chr10:135499271..135513912hg19UCSC Ensembl
chr10:135349261..135363902hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3814642
hg1914642
hg1814642
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv552754, nsv552755
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1503n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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