A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv450686



Internal ID18274486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:347969..501617hg38UCSC Ensembl
Innerchr1:317720..471368hg19UCSC Ensembl
Innerchr1:307583..461231hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38153649
hg19153649
hg18153649
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428223
Supporting Variants
SamplesNA18498
Known GenesLOC100132062, LOC100132287, LOC100133331, OR4F16, OR4F29, OR4F3
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)nssv450686
Frequency
Sample Size62
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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