A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5541n54



Internal ID20138965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:36180353..36217165hg38UCSC Ensembl
chr17:34507719..34544619hg19UCSC Ensembl
chr17:31531832..31568732hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3836813
hg1936901
hg1836901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv574778, nsv574782, nsv574779, nsv574777
Samples
Known GenesCCL3L1, CCL3L3, CCL4L1, CCL4L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5541n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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