A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4494n54



Internal ID22772389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36375572..36423817hg38UCSC Ensembl
chr15:36667773..36716018hg19UCSC Ensembl
chr15:34455065..34503310hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3848246
hg1948246
hg1848246
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv569194, nsv569196
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4494n54
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