A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428222



Internal ID18277986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:109710738..109878614hg38UCSC Ensembl
Innerchr9:112473018..112640894hg19UCSC Ensembl
Innerchr9:111512839..111680715hg18UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38167877
hg19167877
hg18167877
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv451766
SamplesHGDP00449
Known GenesPALM2, PALM2-AKAP2
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)nsv428222
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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