A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5582n100



Internal ID22791669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17472782..17687733hg38UCSC Ensembl
chr5:17472891..17687842hg19UCSC Ensembl
chr5:17525891..17720587hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38214952
hg19214952
hg18194697
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1031345, nsv1034577, nsv1026254, nsv1026651, nsv1024063, nsv1019554, nsv1019396
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5582n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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