A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589745



Internal ID16377154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:13638188..13640208hg38UCSC Ensembl
Innerchr3:13679688..13681708hg19UCSC Ensembl
Innerchr3:13654689..13656709hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg382021
hg192021
hg182021
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8231n54
Supporting Variantsnssv959232, nssv959234, nssv959235, nssv959233
Samples
Known GenesFBLN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589745
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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