A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21910



Internal ID15485294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35358344..35358809hg38UCSC Ensembl
Outerchr19:35357904..35359464hg38UCSC Ensembl
Innerchr19:35849246..35849711hg19UCSC Ensembl
Outerchr19:35848806..35850366hg19UCSC Ensembl
Innerchr19:40541086..40541551hg18UCSC Ensembl
Outerchr19:40540646..40542206hg18UCSC Ensembl
Innerchr19:40541086..40541551hg17UCSC Ensembl
Outerchr19:40540646..40542206hg17UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg381561
hg191561
hg181561
hg171561
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9712
Supporting Variants
SamplesNA12802
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)nssv21910
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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