A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5475n54



Internal ID18997651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:16491622..16492366hg38UCSC Ensembl
chr17:16394936..16395680hg19UCSC Ensembl
chr17:16335661..16336405hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38745
hg19745
hg18745
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv574490, nsv574491, nsv574493, nsv574489
Samples
Known GenesFAM211A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5475n54
Frequency
Sample Size17421
Observed Gain18
Observed Loss0
Observed Complex0
Frequencyn/a


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