A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18715



Internal ID15840770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46720813..46738122hg38UCSC Ensembl
Outerchr10:46720543..46738301hg38UCSC Ensembl
Innerchr10:48119769..48137058hg19UCSC Ensembl
Outerchr10:48119499..48137237hg19UCSC Ensembl
Innerchr10:47739775..47757064hg18UCSC Ensembl
Outerchr10:47739505..47757243hg18UCSC Ensembl
Innerchr10:47739775..47757064hg17UCSC Ensembl
Outerchr10:47739505..47757243hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3817759
hg1917739
hg1817739
hg1717739
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA18980
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)nssv18715
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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