A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18355



Internal ID15840605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45826948..45853613hg38UCSC Ensembl
Outerchr10:45826914..45853940hg38UCSC Ensembl
Innerchr10:46322396..46349061hg19UCSC Ensembl
Outerchr10:46322362..46349388hg19UCSC Ensembl
Innerchr10:45642402..45669067hg18UCSC Ensembl
Outerchr10:45642368..45669394hg18UCSC Ensembl
Innerchr10:45642402..45669067hg17UCSC Ensembl
Outerchr10:45642368..45669394hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3827027
hg1927027
hg1827027
hg1727027
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8630
Supporting Variants
SamplesNA18980
Known GenesAGAP4
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)nssv18355
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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