A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9866



Internal ID15847778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:15509584..15925010hg38UCSC Ensembl
Outerchr22:16052999..16468379hg19UCSC Ensembl
Outerchr22:14432999..14848379hg18UCSC Ensembl
Outerchr22:14432999..14842933hg17UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg38415427
hg19415381
hg18415381
hg17409935
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv25324, nssv25034, nssv26286, nssv22115, nssv28062, nssv25352, nssv25787, nssv27261, nssv27069, nssv27079, nssv25738, nssv25663, nssv26652, nssv25860, nssv26223, nssv25050, nssv25809, nssv27870, nssv27647, nssv25839, nssv27884, nssv25685, nssv27238, nssv24781, nssv26075, nssv22541, nssv25025, nssv25830, nssv25377, nssv27890, nssv27877, nssv28065, nssv26242, nssv27655, nssv28721, nssv27788
SamplesNA18502, NA11830, NA18980, NA18504, NA12155, NA18563, NA18860, NA07048, NA18975, NA19007, NA10847, NA10863, NA12872, NA19221, NA18537, NA18853, NA19132, NA18564, NA19240, NA19144, NA12740, NA19173, NA18972, NA18552
Known GenesBMS1P17, BMS1P18, OR11H1, POTEH
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)nsv9866
Frequency
Sample Size31
Observed Gain3
Observed Loss21
Observed Complex0
Frequencyn/a


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