A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9878n54



Internal ID22777773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:73447273..73448317hg38UCSC Ensembl
chr5:72743100..72744142hg19UCSC Ensembl
chr5:72778856..72779898hg18UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg381045
hg191043
hg181043
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv598647, nsv598646
Samples
Known GenesFOXD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9878n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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