A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5792n100



Internal ID22791879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:116260580..116295181hg38UCSC Ensembl
chr5:115596277..115630878hg19UCSC Ensembl
chr5:115624176..115658777hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3834602
hg1934602
hg1834602
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1028664, nsv1020633, nsv1028323, nsv1023495, nsv1015300, nsv1017822, nsv1019259, nsv1018649
Samples
Known GenesCOMMD10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5792n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss87
Observed Complex0
Frequencyn/a


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