A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5728n54



Internal ID22773623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58128727..58136518hg38UCSC Ensembl
chr17:56206088..56213879hg19UCSC Ensembl
chr17:53561087..53568878hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg387792
hg197792
hg187792
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv575767, nsv575766
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5728n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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