A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428361



Internal ID18278125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:4510042..4689189hg38UCSC Ensembl
Innerchr19:4510054..4689201hg19UCSC Ensembl
Innerchr19:4461054..4640201hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38179148
hg19179148
hg18179148
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv453612, nssv453608, nssv453607, nssv453610, nssv453606, nssv453611
SamplesHGDP00474, HGDP00476, HGDP00462, HGDP01094, NA19181, HGDP00471
Known GenesC19orf10, DPP9, LOC100131094, LRG1, PLIN4, PLIN5, SEMA6B, TNFAIP8L1
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)nsv428361
Frequency
Sample Size62
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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