A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9706



Internal ID15847618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:34236108..34240571hg38UCSC Ensembl
Outerchr19:34727013..34731476hg19UCSC Ensembl
Outerchr19:39418853..39423316hg18UCSC Ensembl
Outerchr19:39418853..39423316hg17UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg384464
hg194464
hg184464
hg174464
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv26937, nssv26518, nssv26836, nssv21880, nssv28493, nssv27759, nssv25021, nssv24135, nssv24713, nssv25392, nssv24304, nssv27434, nssv23668, nssv25085, nssv25331, nssv24792, nssv26163, nssv25323, nssv25394, nssv25002, nssv22249, nssv27472, nssv24009, nssv27540, nssv22031, nssv24250
SamplesNA18502, NA11830, NA18980, NA07029, NA18504, NA12155, NA18563, NA12802, NA18860, NA18942, NA07048, NA10839, NA18975, NA19007, NA10863, NA12872, NA18572, NA19221, NA18537, NA18853, NA19132, NA18517, NA18564, NA19240, NA19144, NA12740
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)nsv9706
Frequency
Sample Size31
Observed Gain26
Observed Loss0
Observed Complex0
Frequencyn/a


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