A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9619n54



Internal ID22777514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16179085..16179758hg38UCSC Ensembl
chr5:16179194..16179867hg19UCSC Ensembl
chr5:16232194..16232867hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38674
hg19674
hg18674
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv597298, nsv597303
Samples
Known GenesMARCH11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9619n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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