A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26774



Internal ID15495450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:19101113..19101206hg38UCSC Ensembl
Outerchr17:19100737..19101733hg38UCSC Ensembl
Innerchr17:19004426..19004519hg19UCSC Ensembl
Outerchr17:19004050..19005046hg19UCSC Ensembl
Innerchr17:18945151..18945244hg18UCSC Ensembl
Outerchr17:18944775..18945771hg18UCSC Ensembl
Innerchr17:18945151..18945244hg17UCSC Ensembl
Outerchr17:18944775..18945771hg17UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38997
hg19997
hg18997
hg17997
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)nssv26774
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