A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv514795



Internal ID15466429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:15883901..15884296hg38UCSC Ensembl
Innerchr16:15977758..15978153hg19UCSC Ensembl
Innerchr16:15885259..15885654hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38396
hg19396
hg18396
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2819538, nssv2819537, nssv2819532, nssv2819539, nssv2819530, nssv2819540, nssv2819534, nssv2819533, nssv2819529, nssv2819536, nssv2819541, nssv2819531, nssv2819535
SamplesNA18500, NA19210, NA21425, NA19211, NA19122, NA19103, NA21581, NA19235, NA19101, NA19123, NA19097, NA19095, NA21391
Known GenesFOPNL
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nsv514795
Frequency
Sample Size2366
Observed Gain13
Observed Loss0
Observed Complex0
Frequencyn/a


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