A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9706n54



Internal ID22777601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:28763545..28874006hg38UCSC Ensembl
chr5:28763652..28874113hg19UCSC Ensembl
chr5:28799409..28909870hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg38110462
hg19110462
hg18110462
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv597720, nsv597717, nsv597713, nsv597714, nsv597715
SamplesHGDP00933, HGDP00923, NINDS_222
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9706n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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