A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591820



Internal ID16032543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:133415517..133424474hg38UCSC Ensembl
Innerchr3:133134361..133143318hg19UCSC Ensembl
Innerchr3:134617051..134626008hg18UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg388958
hg198958
hg188958
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv974346
Samples
Known GenesBFSP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591820
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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