A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10045n54



Internal ID22777940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:119362888..119367088hg38UCSC Ensembl
chr5:118698583..118702783hg19UCSC Ensembl
chr5:118726482..118730682hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg384201
hg194201
hg184201
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv599566, nsv599567
Samples
Known GenesTNFAIP8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10045n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer