A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9537



Internal ID15847449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:32060149..32087924hg38UCSC Ensembl
Outerchr17:30387168..30414943hg19UCSC Ensembl
Outerchr17:27411281..27439056hg18UCSC Ensembl
Outerchr17:27411281..27439056hg17UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3827776
hg1927776
hg1827776
hg1727776
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv28227
SamplesNA19221
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)nsv9537
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