A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25895



Internal ID15841579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:82811470..82827413hg38UCSC Ensembl
Outerchr15:82810732..82828076hg38UCSC Ensembl
Innerchr15:83480222..83496165hg19UCSC Ensembl
Outerchr15:83479484..83496828hg19UCSC Ensembl
Innerchr15:81277276..81293219hg18UCSC Ensembl
Outerchr15:81276538..81293882hg18UCSC Ensembl
Innerchr15:81277276..81293219hg17UCSC Ensembl
Outerchr15:81276538..81293882hg17UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3817345
hg1917345
hg1817345
hg1717345
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9288
Supporting Variants
SamplesNA19132
Known GenesWHAMM
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)nssv25895
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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