A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22371



Internal ID15838294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47587753..47588726hg38UCSC Ensembl
Outerchr10:47587739..47588775hg38UCSC Ensembl
Innerchr10:48986696..48987669hg19UCSC Ensembl
Outerchr10:48986682..48987718hg19UCSC Ensembl
Innerchr10:48606702..48607675hg18UCSC Ensembl
Outerchr10:48606688..48607724hg18UCSC Ensembl
Innerchr10:48606702..48607675hg17UCSC Ensembl
Outerchr10:48606688..48607724hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg381037
hg191037
hg181037
hg171037
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA18860
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)nssv22371
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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