A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19217



Internal ID15836054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45675103..45702634hg38UCSC Ensembl
Outerchr10:45674512..45705324hg38UCSC Ensembl
Innerchr10:46170551..46198082hg19UCSC Ensembl
Outerchr10:46169960..46200772hg19UCSC Ensembl
Innerchr10:45490557..45518088hg18UCSC Ensembl
Outerchr10:45489966..45520778hg18UCSC Ensembl
Innerchr10:45490557..45518088hg17UCSC Ensembl
Outerchr10:45489966..45520778hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3830813
hg1930813
hg1830813
hg1730813
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8628
Supporting Variants
SamplesNA18563
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)nssv19217
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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