A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21983



Internal ID15839535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46737635..46779804hg38UCSC Ensembl
Outerchr10:46737409..46780289hg38UCSC Ensembl
Innerchr10:46769823..46811982hg19UCSC Ensembl
Outerchr10:46769338..46812208hg19UCSC Ensembl
Innerchr10:46189829..46231988hg18UCSC Ensembl
Outerchr10:46189344..46232214hg18UCSC Ensembl
Innerchr10:46189829..46231988hg17UCSC Ensembl
Outerchr10:46189344..46232214hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3842881
hg1942871
hg1842871
hg1742871
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8636
Supporting Variants
SamplesNA18972
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)nssv21983
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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