A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589742



Internal ID16377151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:13637835..13640157hg38UCSC Ensembl
Innerchr3:13679335..13681657hg19UCSC Ensembl
Innerchr3:13654336..13656658hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg382323
hg192323
hg182323
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8231n54
Supporting Variantsnssv959227
Samples
Known GenesFBLN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589742
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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