A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428263



Internal ID18624713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:86646948..86797438hg38UCSC Ensembl
Innerchr11:86357990..86508480hg19UCSC Ensembl
Innerchr11:86035638..86186128hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38150491
hg19150491
hg18150491
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv452138, nssv452139, nssv452140, nssv452137, nssv452136
SamplesHGDP00476, HGDP00450, NA19181, NA19113, HGDP00474
Known GenesME3
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)nsv428263
Frequency
Sample Size62
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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