A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5544n54



Internal ID20138968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:36201388..36211948hg38UCSC Ensembl
chr17:34528788..34539350hg19UCSC Ensembl
chr17:31552901..31563463hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3810561
hg1910563
hg1810563
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv574787, nsv574794, nsv574786, nsv574791, nsv574793, nsv574808
Samples
Known GenesCCL4L1, CCL4L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5544n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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