A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5533n54



Internal ID22773428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35404745..35433147hg38UCSC Ensembl
chr17:33731764..33760166hg19UCSC Ensembl
chr17:30755877..30784279hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3828403
hg1928403
hg1828403
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv574752, nsv574753
Samples
Known GenesSLFN12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5533n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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