A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8023



Internal ID15499249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:13090..80755hg38UCSC Ensembl
Outerchr7:13090..80755hg19UCSC Ensembl
Outerchr7:105852..175838hg18UCSC Ensembl
Outerchr7:105852..175838hg17UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3867666
hg1967666
hg1869987
hg1769987
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15303, nssv16692, nssv15258, nssv15333, nssv15334, nssv15364, nssv13879, nssv14930, nssv16058, nssv14906, nssv17834, nssv14807, nssv15599, nssv14705, nssv17187, nssv17804, nssv14900, nssv15576, nssv17157, nssv14604, nssv15939
SamplesNA18502, NA12155, NA18563, NA07048, NA10839, NA18975, NA19007, NA10847, NA10863, NA18572, NA18853, NA19132, NA18517, NA18564, NA12740, NA19173
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)nsv8023
Frequency
Sample Size31
Observed Gain8
Observed Loss11
Observed Complex0
Frequencyn/a


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