A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5764n54



Internal ID20139188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:72819082..72822670hg38UCSC Ensembl
chr17:70815221..70818809hg19UCSC Ensembl
chr17:68326816..68330404hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg383589
hg193589
hg183589
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv575968, nsv575970, nsv575969, nsv575964, nsv575976, nsv575965
Samples
Known GenesSLC39A11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5764n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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