A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7659n54



Internal ID22775554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62951856..62968122hg38UCSC Ensembl
chr20:61583208..61599474hg19UCSC Ensembl
chr20:61053653..61069919hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3816267
hg1916267
hg1816267
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586533, nsv586534
Samples1780862021_A
Known GenesSLC17A9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7659n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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