A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21657



Internal ID15841749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45678845..45706692hg38UCSC Ensembl
Outerchr10:45678733..45707726hg38UCSC Ensembl
Innerchr10:46174293..46202140hg19UCSC Ensembl
Outerchr10:46174181..46203174hg19UCSC Ensembl
Innerchr10:45494299..45522146hg18UCSC Ensembl
Outerchr10:45494187..45523180hg18UCSC Ensembl
Innerchr10:45494299..45522146hg17UCSC Ensembl
Outerchr10:45494187..45523180hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3828994
hg1928994
hg1828994
hg1728994
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8628
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)nssv21657
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