A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9624n54



Internal ID22777519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17351166..17356505hg38UCSC Ensembl
chr5:17351275..17356614hg19UCSC Ensembl
chr5:17404275..17409614hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg385340
hg195340
hg185340
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv597327, nsv597324, nsv597328, nsv597325, nsv597326, nsv597329, nsv597323
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9624n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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