A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545416



Internal ID15986139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:11620226..11676353hg38UCSC Ensembl
Innerchr1:11680283..11736410hg19UCSC Ensembl
Innerchr1:11602870..11658997hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3856128
hg1956128
hg1856128
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv709935
Samples
Known GenesFBXO2, FBXO44, FBXO6, MAD2L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545416
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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