A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428158



Internal ID18624608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:170272663..170700831hg38UCSC Ensembl
Innerchr6:170581751..171009919hg19UCSC Ensembl
Innerchr6:170423676..170851844hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38428169
hg19428169
hg18428169
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv450896, nssv450895
SamplesNA19181, NA19096
Known GenesDLL1, FAM120B, FLJ38122, MIR4644, PDCD2, PSMB1, TBP
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)nsv428158
Frequency
Sample Size62
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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