A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10623



Internal ID15845586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:184235214..184250967hg38UCSC Ensembl
Outerchr4:185156367..185172120hg19UCSC Ensembl
Outerchr4:185393361..185409114hg18UCSC Ensembl
Outerchr4:185531516..185547269hg17UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3815754
hg1915754
hg1815754
hg1715754
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv12345, nssv12999, nssv12898, nssv13289, nssv13902, nssv12834, nssv14023, nssv12315, nssv14970, nssv12407, nssv12740, nssv13977, nssv12496, nssv11719, nssv12306, nssv12964, nssv12596, nssv12805, nssv12065, nssv12487, nssv12969, nssv14024, nssv11951, nssv13381, nssv14053, nssv12482, nssv11830, nssv12035, nssv12452, nssv13994, nssv11689, nssv11800, nssv14001, nssv13023, nssv12948, nssv12276, nssv13778, nssv14573, nssv12412
SamplesNA18502, NA11830, NA18980, NA07029, NA18504, NA12155, NA18563, NA12802, NA18860, NA18942, NA07048, NA10839, NA18975, NA19007, NA10847, NA10863, NA12872, NA18572, NA19221, NA18537, NA18853, NA19132, NA18517, NA18564, NA19240, NA19144, NA12740, NA19173, NA18972, NA18552
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)nsv10623
Frequency
Sample Size31
Observed Gain30
Observed Loss0
Observed Complex0
Frequencyn/a


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