A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12868n54



Internal ID20146292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126572421..126646919hg38UCSC Ensembl
chr9:129334700..129409198hg19UCSC Ensembl
chr9:128374521..128449019hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3874499
hg1974499
hg1874499
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv615313, nsv615312
Samples
Known GenesLMX1B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12868n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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