A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9993n54



Internal ID22777888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:106020189..106077397hg38UCSC Ensembl
chr5:105355890..105413098hg19UCSC Ensembl
chr5:105383789..105440997hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3857209
hg1957209
hg1857209
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv599286, nsv599287, nsv599284, nsv599283
SamplesHGDP00738, HGDP00926, HGDP01345
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9993n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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