A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591613



Internal ID16379022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:128661938..128694054hg38UCSC Ensembl
Innerchr3:128380781..128412897hg19UCSC Ensembl
Innerchr3:129863471..129895587hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3832117
hg1932117
hg1832117
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8569n54
Supporting Variantsnssv972998, nssv973005, nssv973006, nssv973003, nssv972986, nssv972980, nssv972982, nssv972995, nssv972987, nssv972984, nssv972981, nssv972991, nssv973000, nssv973001, nssv972992, nssv973004, nssv972993, nssv972990, nssv972985, nssv972983, nssv972988, nssv973002, nssv972997, nssv972994, nssv972999, nssv972989, nssv972996
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591613
Frequency
Sample Size17421
Observed Gain27
Observed Loss0
Observed Complex0
Frequencyn/a


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