A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3454n54



Internal ID22771349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113799443..113803777hg38UCSC Ensembl
chr13:114502416..114506750hg19UCSC Ensembl
chr13:113607193..113611527hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg384335
hg194335
hg184335
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv563412, nsv563418, nsv563405
Samples
Known GenesTMEM255B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3454n54
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