A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10329



Internal ID15845292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:138084501..138088274hg38UCSC Ensembl
Outerchr3:137803343..137807116hg19UCSC Ensembl
Outerchr3:139286033..139289806hg18UCSC Ensembl
Outerchr3:139286041..139289814hg17UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg383774
hg193774
hg183774
hg173774
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv28909, nssv29005, nssv11641, nssv11909, nssv28668, nssv12192, nssv11574, nssv28877, nssv12163
SamplesNA18502, NA18504, NA18942, NA18975, NA18572, NA18853, NA19240, NA19144, NA19173
Known GenesDZIP1L
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)nsv10329
Frequency
Sample Size31
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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