A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428264



Internal ID18624714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:91051766..91186887hg38UCSC Ensembl
Innerchr11:90784934..90920055hg19UCSC Ensembl
Innerchr11:90424582..90559703hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38135122
hg19135122
hg18135122
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv452201, nssv452202, nssv452200, nssv452180, nssv452188, nssv452196, nssv452194, nssv452187, nssv452185, nssv452179, nssv452204, nssv452181, nssv452191, nssv452192, nssv452193, nssv452198, nssv452195, nssv452203, nssv452199, nssv452189, nssv452182, nssv452183, nssv452178, nssv452190, nssv452184
SamplesHGDP01087, HGDP00462, HGDP00463, HGDP01088, HGDP01089, NA18498, HGDP00476, NA19189, HGDP00460, HGDP00450, HGDP00473, HGDP00986, HGDP00467, NA19113, NA19257, NA19225, NA19108, NA19147, HGDP01094, HGDP00984, HGDP00472, HGDP00474, NA19096, HGDP00478, HGDP00449
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)nsv428264
Frequency
Sample Size62
Observed Gain25
Observed Loss0
Observed Complex0
Frequencyn/a


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