A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv454089



Internal ID18275253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:129818076..130109402hg38UCSC Ensembl
Innerchr2:130575649..130866975hg19UCSC Ensembl
Innerchr2:130292119..130583445hg18UCSC Ensembl
Cytoband2q21.1
Allele length
AssemblyAllele length
hg38291327
hg19291327
hg18291327
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428403
Supporting Variants
SamplesNA19225
Known GenesFAR2P1, LOC389033, POTEF, RAB6C, RAB6C-AS1
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)nssv454089
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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