A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591614



Internal ID16379023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:128661938..128694721hg38UCSC Ensembl
Innerchr3:128380781..128413564hg19UCSC Ensembl
Innerchr3:129863471..129896254hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3832784
hg1932784
hg1832784
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8569n54
Supporting Variantsnssv973011, nssv973009, nssv973013, nssv973008, nssv973007, nssv973012, nssv973010, nssv973014
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591614
Frequency
Sample Size17421
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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