A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv453737



Internal ID18274926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:47966570..48039659hg38UCSC Ensembl
Innerchr19:48469827..48542916hg19UCSC Ensembl
Innerchr19:53161639..53234728hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3873090
hg1973090
hg1873090
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428367
Supporting Variants
SamplesNA19113
Known GenesBSPH1, CABP5, ELSPBP1
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)nssv453737
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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