A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8731



Internal ID15846643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:122579399..122622194hg38UCSC Ensembl
Outerchr10:124338915..124381710hg19UCSC Ensembl
Outerchr10:124328905..124371700hg18UCSC Ensembl
Outerchr10:124328905..124371700hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3842796
hg1942796
hg1842796
hg1742796
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv19250, nssv19236, nssv22583, nssv19276, nssv18804, nssv22553, nssv19534, nssv19533, nssv20287, nssv19739, nssv19615, nssv19899, nssv19226, nssv22257, nssv19196, nssv21852, nssv17869, nssv19564, nssv20578, nssv19929, nssv19645, nssv18512, nssv22124, nssv21792, nssv18482, nssv18834, nssv17855, nssv24673, nssv21373, nssv19545, nssv21822, nssv23047, nssv17932, nssv19668, nssv19280, nssv17620, nssv17839, nssv22154, nssv19997, nssv20318, nssv19575, nssv20317, nssv19246, nssv17561, nssv21463, nssv21751, nssv22227, nssv20027
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 GenesDMBT1
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)nsv8731
Frequency
Sample Size31
Observed Gain23
Observed Loss19
Observed Complex0
Frequencyn/a


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