A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428150



Internal ID18624600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:92699750..92877560hg38UCSC Ensembl
Innerchr6:93409468..93587278hg19UCSC Ensembl
Innerchr6:93466189..93643999hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38177811
hg19177811
hg18177811
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv450806
SamplesHGDP01087
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)nsv428150
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer