A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17302



Internal ID15839055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46840138..46840508hg38UCSC Ensembl
Outerchr10:46840057..46841068hg38UCSC Ensembl
Innerchr10:46712321..46712691hg19UCSC Ensembl
Outerchr10:46711761..46712772hg19UCSC Ensembl
Innerchr10:46132327..46132697hg18UCSC Ensembl
Outerchr10:46131767..46132778hg18UCSC Ensembl
Innerchr10:46132327..46132697hg17UCSC Ensembl
Outerchr10:46131767..46132778hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg381012
hg191012
hg181012
hg171012
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA18942
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)nssv17302
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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