A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428352



Internal ID18624802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:1915708..2172954hg38UCSC Ensembl
Innerchr18:1915709..2172954hg19UCSC Ensembl
Innerchr18:1905709..2162954hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38257247
hg19257246
hg18257246
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv453571, nssv453572
SamplesHGDP01094, HGDP00472
Known Genes
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)nsv428352
Frequency
Sample Size62
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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