A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428216



Internal ID18624666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62798833..62958371hg38UCSC Ensembl
Innerchr9:66454657..66614195hg19UCSC Ensembl
Innerchr9:66194477..66354015hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38159539
hg19159539
hg18159539
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv451736, nssv451735
SamplesHGDP00476, NA19113
Known GenesMGC21881, PTGER4P2-CDK2AP2P2
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)nsv428216
Frequency
Sample Size62
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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