A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546847



Internal ID15987570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:93824138..93825696hg38UCSC Ensembl
Innerchr1:94289694..94291252hg19UCSC Ensembl
Innerchr1:94062282..94063840hg18UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg381559
hg191559
hg181559
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv374n54
Supporting Variantsnssv719610
Samples
Known GenesBCAR3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546847
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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