A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25260



Internal ID15496688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46356830..46487908hg38UCSC Ensembl
Outerchr17:46355322..46489958hg38UCSC Ensembl
Innerchr17:44434196..44565274hg19UCSC Ensembl
Outerchr17:44432688..44567324hg19UCSC Ensembl
Innerchr17:41789936..41920590hg18UCSC Ensembl
Outerchr17:41788428..41922640hg18UCSC Ensembl
Innerchr17:41789936..41920590hg17UCSC Ensembl
Outerchr17:41788428..41922640hg17UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38134637
hg19134637
hg18134213
hg17134213
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9564
Supporting Variants
SamplesNA19173
Known GenesARL17A, ARL17B, NSFP1
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)nssv25260
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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