A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv370n54



Internal ID18992546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:93822968..93828936hg38UCSC Ensembl
chr1:94288524..94294492hg19UCSC Ensembl
chr1:94061112..94067080hg18UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg385969
hg195969
hg185969
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv546832, nsv546831
Samples
Known GenesBCAR3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv370n54
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