A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10063n54



Internal ID22777958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:128000341..128013018hg38UCSC Ensembl
chr5:127336033..127348710hg19UCSC Ensembl
chr5:127363932..127376609hg18UCSC Ensembl
Cytoband5q23.3
Allele length
AssemblyAllele length
hg3812678
hg1912678
hg1812678
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv599669, nsv599668, nsv599667
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10063n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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