A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10715



Internal ID15845678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:94566245..94572757hg38UCSC Ensembl
Outerchr5:93901950..93908462hg19UCSC Ensembl
Outerchr5:93927706..93934218hg18UCSC Ensembl
Outerchr5:93927706..93934218hg17UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg386513
hg196513
hg186513
hg176513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14559, nssv12581, nssv13655, nssv13545, nssv14043, nssv13307, nssv13644, nssv14044, nssv13876, nssv15923, nssv13382, nssv13580, nssv14491, nssv13798, nssv15614, nssv13926, nssv14039
SamplesNA07029, NA18563, NA07048, NA10839, NA18975, NA10847, NA10863, NA12872, NA18537, NA18853, NA18517, NA19240, NA19144, NA12740, NA19173, NA18972, NA18552
Known GenesKIAA0825
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)nsv10715
Frequency
Sample Size31
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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