A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19010



Internal ID15837404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:68853554..68860824hg38UCSC Ensembl
Outerchr10:68852817..68868800hg38UCSC Ensembl
Innerchr10:70613310..70620580hg19UCSC Ensembl
Outerchr10:70612573..70628556hg19UCSC Ensembl
Innerchr10:70283316..70290586hg18UCSC Ensembl
Outerchr10:70282579..70298562hg18UCSC Ensembl
Innerchr10:70283316..70290586hg17UCSC Ensembl
Outerchr10:70282579..70298562hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3815984
hg1915984
hg1815984
hg1715984
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8685
Supporting Variants
SamplesNA18853
Known GenesSTOX1
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)nssv19010
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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