A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428155



Internal ID18624605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160516284..160658766hg38UCSC Ensembl
Innerchr6:160937316..161079798hg19UCSC Ensembl
Innerchr6:160857306..160999788hg18UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38142483
hg19142483
hg18142483
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv450870, nssv450872, nssv450866, nssv450865, nssv450861, nssv450869, nssv450878, nssv450868, nssv450879, nssv450863, nssv450874, nssv450862, nssv450871, nssv450880, nssv450877, nssv450876, nssv450867, nssv450882, nssv450881, nssv450873
SamplesHGDP01087, HGDP01093, HGDP01088, HGDP01089, NA18498, HGDP00476, NA19189, HGDP00473, HGDP00986, NA19257, NA19225, NA19108, NA19147, HGDP01094, HGDP00984, HGDP00472, HGDP00474, HGDP00471, HGDP00478, HGDP01086
Known GenesLPA
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)nsv428155
Frequency
Sample Size62
Observed Gain20
Observed Loss0
Observed Complex0
Frequencyn/a


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