A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv514908



Internal ID15466542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:9752742..9760415hg38UCSC Ensembl
Innerchr19:9863418..9871091hg19UCSC Ensembl
Innerchr19:9724418..9732091hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg387674
hg197674
hg187674
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2843658, nssv2843654, nssv2843655, nssv2843641, nssv2843645, nssv2843643, nssv2843647, nssv2843653, nssv2843646, nssv2843657, nssv2843639, nssv2843651, nssv2843652, nssv2843642, nssv2843650, nssv2843640, nssv2843656, nssv2843648, nssv2843649, nssv2843638, nssv2843644
SamplesNA19142, NA21634, NA19127, NA19173, NA19252, NA21718, NA18484, NA18488, NA21716, NA19153, NA19122, NA19129, NA19154, NA19141, NA19235, NA19116, NA19097, NA18852, NA21583, NA19095, NA19171
Known GenesZNF846
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nsv514908
Frequency
Sample Size2366
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


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