A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546835



Internal ID15987558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:93823114..93824784hg38UCSC Ensembl
Innerchr1:94288670..94290340hg19UCSC Ensembl
Innerchr1:94061258..94062928hg18UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg381671
hg191671
hg181671
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv371n54
Supporting Variantsnssv719593
Samples
Known GenesBCAR3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546835
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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