A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591346



Internal ID16378755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:116607951..116635978hg38UCSC Ensembl
Innerchr3:116326798..116354825hg19UCSC Ensembl
Innerchr3:117809488..117837515hg18UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3828028
hg1928028
hg1828028
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152530
Samples1780854279_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591346
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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