A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv514890



Internal ID15813249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14805077..14811820hg38UCSC Ensembl
Innerchr19:14915889..14922632hg19UCSC Ensembl
Innerchr19:14776889..14783632hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg386744
hg196744
hg186744
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2841376, nssv2841369, nssv2841378, nssv2841373, nssv2841375, nssv2841377, nssv2841371, nssv2841368, nssv2841374, nssv2841370, nssv2841372
SamplesNA19186, NA19204, NA18868, NA19175, NA19184, NA19205, NA18856, NA19113, NA18857, NA18869, NA19185
Known Genes
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nsv514890
Frequency
Sample Size2366
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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