A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv451358



Internal ID18621319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:96943..186362hg38UCSC Ensembl
Innerchr8:46943..136362hg19UCSC Ensembl
Innerchr8:36943..126362hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3889420
hg1989420
hg1889420
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428193
Supporting Variants
SamplesNA19096
Known GenesOR4F21
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)nssv451358
Frequency
Sample Size62
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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