A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv451665



Internal ID18621891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:37977890..38154218hg38UCSC Ensembl
Innerchr9:37977887..38154215hg19UCSC Ensembl
Innerchr9:37967887..38144215hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38176329
hg19176329
hg18176329
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428210
Supporting Variants
SamplesNA19225
Known GenesSHB
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)nssv451665
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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