A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589743



Internal ID16377152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:13637835..13640208hg38UCSC Ensembl
Innerchr3:13679335..13681708hg19UCSC Ensembl
Innerchr3:13654336..13656709hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg382374
hg192374
hg182374
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8231n54
Supporting Variantsnssv959230, nssv959229, nssv959228
Samples
Known GenesFBLN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589743
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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