A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5912n100



Internal ID20157528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:5132027..5431352hg38UCSC Ensembl
chr6:5132261..5431585hg19UCSC Ensembl
chr6:5077260..5376584hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38299326
hg19299325
hg18299325
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1029609, nsv1030254
Samples
Known GenesFARS2, LYRM4, MIR3691
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5912n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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