A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26771



Internal ID15834108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:806669..807287hg38UCSC Ensembl
Outerchr17:805972..807906hg38UCSC Ensembl
Innerchr17:709909..710527hg19UCSC Ensembl
Outerchr17:709212..711146hg19UCSC Ensembl
Innerchr17:656659..657277hg18UCSC Ensembl
Outerchr17:655962..657896hg18UCSC Ensembl
Innerchr17:656659..657277hg17UCSC Ensembl
Outerchr17:655962..657896hg17UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg381935
hg191935
hg181935
hg171935
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9486
Supporting Variants
SamplesNA18517
Known GenesNXN
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)nssv26771
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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