A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9713n54



Internal ID22777608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:28935946..29145548hg38UCSC Ensembl
chr5:28936053..29145655hg19UCSC Ensembl
chr5:28971810..29181412hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38209603
hg19209603
hg18209603
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv597750, nsv597751
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9713n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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