A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428418



Internal ID18278182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75566792..75924423hg38UCSC Ensembl
Innerchr3:75615943..75973574hg19UCSC Ensembl
Innerchr3:75698633..76056264hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38357632
hg19357632
hg18357632
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv454252, nssv454253
SamplesHGDP01093, HGDP00476
Known GenesFLJ20518, FRG2C, LINC00960, MIR1324, MIR4273, ZNF717
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)nsv428418
Frequency
Sample Size62
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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