A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26796



Internal ID15495367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:19227281..19227374hg38UCSC Ensembl
Outerchr17:19226780..19227901hg38UCSC Ensembl
Innerchr17:19130594..19130687hg19UCSC Ensembl
Outerchr17:19130093..19131214hg19UCSC Ensembl
Innerchr17:19071187..19071280hg18UCSC Ensembl
Outerchr17:19070686..19071807hg18UCSC Ensembl
Innerchr17:19071187..19071280hg17UCSC Ensembl
Outerchr17:19070686..19071807hg17UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg381122
hg191122
hg181122
hg171122
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9504
Supporting Variants
SamplesNA19132
Known Genes
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)nssv26796
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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