A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428448



Internal ID18624898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:114085964..114507673hg38UCSC Ensembl
Innerchr4:115007120..115428829hg19UCSC Ensembl
Innerchr4:115226569..115648278hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38421710
hg19421710
hg18421710
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv454579, nssv454574, nssv454575, nssv454573, nssv454578, nssv454577
SamplesHGDP01093, NA19189, NA19181, NA19113, NA19147, HGDP01094
Known Genes
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)nsv428448
Frequency
Sample Size62
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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