A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428266



Internal ID18278030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:131562907..131879091hg38UCSC Ensembl
Innerchr11:131432801..131748985hg19UCSC Ensembl
Innerchr11:130938011..131254195hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38316185
hg19316185
hg18316185
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv452210, nssv452211, nssv452212, nssv452214, nssv452213
SamplesHGDP00474, NA19189, HGDP00467, NA18498, NA19113
Known GenesNTM
MethodBAC aCGH
AnalysisCopy number variable segments were automatically detected using the CNVfinder algorithm (Fiegler et al. 2006).
PlatformSanger H. sapiens Whole Genome Tile Path 28.7k v3
Comments
ReferencePerry_et_al_2008b
Pubmed ID18775914
Accession Number(s)nsv428266
Frequency
Sample Size62
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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