A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4587n54



Internal ID22772482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71183376..71185709hg38UCSC Ensembl
chr15:71475715..71478048hg19UCSC Ensembl
chr15:69262769..69265102hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg382334
hg192334
hg182334
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv569825, nsv569827, nsv569824, nsv569826, nsv569829
Samples
Known GenesTHSD4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4587n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss38
Observed Complex0
Frequencyn/a


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