A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428374



Internal ID18278138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1496135..1698610hg38UCSC Ensembl
Innerchr20:1476781..1679256hg19UCSC Ensembl
Innerchr20:1424781..1627256hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38202476
hg19202476
hg18202476
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv453822, nssv453821, nssv453817, nssv453819, nssv453824, nssv453823, nssv453825, nssv453818, nssv453816
SamplesHGDP00463, NA19189, HGDP00986, NA19113, NA19147, HGDP01094, HGDP00471, NA19096, HGDP00449
Known GenesSIRPB1, SIRPD, SIRPG
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)nsv428374
Frequency
Sample Size62
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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