A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515126



Internal ID15466760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:129764204..129765660hg38UCSC Ensembl
Innerchr9:132526483..132527939hg19UCSC Ensembl
Innerchr9:131566304..131567760hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg381457
hg191457
hg181457
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2970571, nssv2970573, nssv2970577, nssv2970579, nssv2970572, nssv2970583, nssv2970574, nssv2970585, nssv2970581, nssv2970570, nssv2970582, nssv2970575, nssv2970584, nssv2970580, nssv2970578, nssv2970576, nssv2970569
SamplesNA21403, NA21635, NA19127, NA19201, NA19119, NA19138, NA19128, NA18908, NA18910, NA18503, NA19202, NA19108, NA21615, NA18911, NA21404, NA19129, NA19214
Known Genes
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nsv515126
Frequency
Sample Size2366
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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