A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8243n54



Internal ID22776138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16197487..16200987hg38UCSC Ensembl
chr3:16238994..16242494hg19UCSC Ensembl
chr3:16213998..16217498hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg383501
hg193501
hg183501
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv589817, nsv589825, nsv589824, nsv589826
Samples
Known GenesGALNT15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8243n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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