A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428154



Internal ID18624604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:132950836..133201664hg38UCSC Ensembl
Innerchr6:133271975..133522803hg19UCSC Ensembl
Innerchr6:133313668..133564496hg18UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38250829
hg19250829
hg18250829
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv450851
SamplesNA19147
Known GenesLINC00326
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)nsv428154
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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