A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428226



Internal ID18277990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133959913..134129484hg38UCSC Ensembl
Innerchr9:136825035..136994606hg19UCSC Ensembl
Innerchr9:135814856..135984427hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38169572
hg19169572
hg18169572
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv451778
SamplesHGDP00449
Known GenesBRD3, LINC00094, VAV2
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)nsv428226
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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