A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21882



Internal ID15833067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:123433569..123434223hg38UCSC Ensembl
Outerchr10:123432948..123435121hg38UCSC Ensembl
Innerchr10:125193085..125193739hg19UCSC Ensembl
Outerchr10:125192464..125194637hg19UCSC Ensembl
Innerchr10:125183075..125183729hg18UCSC Ensembl
Outerchr10:125182454..125184627hg18UCSC Ensembl
Innerchr10:125183075..125183729hg17UCSC Ensembl
Outerchr10:125182454..125184627hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg382174
hg192174
hg182174
hg172174
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8733
Supporting Variants
SamplesNA18502
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)nssv21882
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