A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17599



Internal ID15490639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:79714514..79741624hg38UCSC Ensembl
Outerchr10:79713231..79746090hg38UCSC Ensembl
Innerchr10:81474270..81501380hg19UCSC Ensembl
Outerchr10:81472987..81505846hg19UCSC Ensembl
Innerchr10:81144276..81171386hg18UCSC Ensembl
Outerchr10:81142993..81175852hg18UCSC Ensembl
Innerchr10:81144276..81171386hg17UCSC Ensembl
Outerchr10:81142993..81175852hg17UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3832860
hg1932860
hg1832860
hg1732860
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8697
Supporting Variants
SamplesNA18572
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)nssv17599
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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