A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24330



Internal ID15481501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35358344..35373018hg38UCSC Ensembl
Outerchr19:35357904..35373505hg38UCSC Ensembl
Innerchr19:35849246..35863920hg19UCSC Ensembl
Outerchr19:35848806..35864407hg19UCSC Ensembl
Innerchr19:40541086..40555760hg18UCSC Ensembl
Outerchr19:40540646..40556247hg18UCSC Ensembl
Innerchr19:40541086..40555760hg17UCSC Ensembl
Outerchr19:40540646..40556247hg17UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3815602
hg1915602
hg1815602
hg1715602
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9712
Supporting Variants
SamplesNA07048
Known GenesFFAR3
MethodOligo aCGH
AnalysisStatistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2
PlatformAgilent-015686 Custom Human 244K CGH Microarray
Comments
ReferencePerry_et_al_2008
Pubmed ID18304495
Accession Number(s)nssv24330
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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