A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4787n54



Internal ID22772682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100879459..100880220hg38UCSC Ensembl
chr15:101419664..101420425hg19UCSC Ensembl
chr15:99237187..99237948hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38762
hg19762
hg18762
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv570822, nsv570823, nsv570820
Samples
Known GenesALDH1A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4787n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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