A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10314



Internal ID15845277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:125952046..125959776hg38UCSC Ensembl
Outerchr3:125670889..125678619hg19UCSC Ensembl
Outerchr3:127153579..127161309hg18UCSC Ensembl
Outerchr3:127153587..127161317hg17UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg387731
hg197731
hg187731
hg177731
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv12810, nssv12923, nssv11611, nssv28847, nssv11514, nssv11879, nssv12278, nssv12132, nssv28620, nssv12081, nssv12254
SamplesNA18502, NA12155, NA18860, NA18975, NA12872, NA19221, NA18853, NA18517, NA19240, NA19173, NA18972
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)nsv10314
Frequency
Sample Size31
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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