A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5748n54



Internal ID22773643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:66074410..66153058hg38UCSC Ensembl
chr17:64070528..64149176hg19UCSC Ensembl
chr17:61500990..61579638hg18UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg3878649
hg1978649
hg1878649
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv575886, nsv575885, nsv575887
SamplesHGDP01325
Known GenesCEP112
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5748n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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