A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5606n100



Internal ID22791693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:24778255..24790740hg38UCSC Ensembl
chr5:24778364..24790849hg19UCSC Ensembl
chr5:24814121..24826606hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3812486
hg1912486
hg1812486
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1016850, nsv1025303, nsv1028046
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)dgv5606n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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