A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26833



Internal ID15498207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:23253767..23255349hg38UCSC Ensembl
Outerchr19:23252066..23256885hg38UCSC Ensembl
Innerchr19:23436569..23438151hg19UCSC Ensembl
Outerchr19:23434868..23439687hg19UCSC Ensembl
Innerchr19:23228409..23229991hg18UCSC Ensembl
Outerchr19:23226708..23231527hg18UCSC Ensembl
Innerchr19:23228409..23229991hg17UCSC Ensembl
Outerchr19:23226708..23231527hg17UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg384820
hg194820
hg184820
hg174820
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9686
Supporting Variants
SamplesNA19240
Known GenesLOC100132815
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)nssv26833
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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