A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9885n54



Internal ID20143309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:76790772..76834288hg38UCSC Ensembl
chr5:76086597..76130113hg19UCSC Ensembl
chr5:76122353..76165869hg18UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3843517
hg1943517
hg1843517
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv598684, nsv598685, nsv598683
Samples
Known GenesF2RL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9885n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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