A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18325



Internal ID15840581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45678733..45705324hg38UCSC Ensembl
Outerchr10:45678719..45706380hg38UCSC Ensembl
Innerchr10:46174181..46200772hg19UCSC Ensembl
Outerchr10:46174167..46201828hg19UCSC Ensembl
Innerchr10:45494187..45520778hg18UCSC Ensembl
Outerchr10:45494173..45521834hg18UCSC Ensembl
Innerchr10:45494187..45520778hg17UCSC Ensembl
Outerchr10:45494173..45521834hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3827662
hg1927662
hg1827662
hg1727662
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8628
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)nssv18325
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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