A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10491



Internal ID15845454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:49520442..49628773hg38UCSC Ensembl
Outerchr4:49522459..49630790hg19UCSC Ensembl
Outerchr4:49217216..49325547hg18UCSC Ensembl
Outerchr4:49363387..49471718hg17UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg38108332
hg19108332
hg18108332
hg17108332
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13212, nssv11896, nssv13148, nssv12184, nssv11835, nssv11926, nssv12086, nssv11646, nssv13124, nssv11672, nssv13913, nssv12951
SamplesNA18502, NA07029, NA12155, NA18860, NA10839, NA19007, NA10863, NA18537, NA18517, 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)nsv10491
Frequency
Sample Size31
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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