A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv20899



Internal ID15490463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:19098173..19098193hg38UCSC Ensembl
Outerchr17:19097258..19099138hg38UCSC Ensembl
Innerchr17:19001486..19001506hg19UCSC Ensembl
Outerchr17:19000571..19002451hg19UCSC Ensembl
Innerchr17:18942211..18942231hg18UCSC Ensembl
Outerchr17:18941296..18943176hg18UCSC Ensembl
Innerchr17:18942211..18942231hg17UCSC Ensembl
Outerchr17:18941296..18943176hg17UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg381881
hg191881
hg181881
hg171881
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9504
Supporting Variants
SamplesNA18572
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)nssv20899
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer