A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11245n54



Internal ID20144669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:28533947..28535389hg38UCSC Ensembl
chr7:28573565..28575007hg19UCSC Ensembl
chr7:28540090..28541532hg18UCSC Ensembl
Cytoband7p15.1
Allele length
AssemblyAllele length
hg381443
hg191443
hg181443
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv606472, nsv606471
Samples
Known GenesCREB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11245n54
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