A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4418n54



Internal ID22772313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30194842..30395361hg38UCSC Ensembl
chr15:30487045..30687564hg19UCSC Ensembl
chr15:28274337..28474856hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38200520
hg19200520
hg18200520
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv568721, nsv568722, nsv568732, nsv568729
Samples
Known GenesCHRFAM7A, DKFZP434L187
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4418n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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