A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv514772



Internal ID15813131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24861870..24863546hg38UCSC Ensembl
Innerchr15:25107017..25108693hg19UCSC Ensembl
Innerchr15:22658110..22659786hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381677
hg191677
hg181677
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2808567, nssv2809865, nssv2810014, nssv2815098, nssv2811753, nssv2810519, nssv2813252, nssv2814882, nssv2809075, nssv2814985, nssv2816306, nssv2810140, nssv2818153, nssv2815976, nssv2808504, nssv2815151, nssv2814117, nssv2810484, nssv2810080, nssv2816171, nssv2816652, nssv2814236, nssv2814750, nssv2808586, nssv2814649, nssv2812813, nssv2814237, nssv2808958, nssv2816883, nssv2808825, nssv2816830, nssv2816144, nssv2818442, nssv2809046, nssv2809398, nssv2810625, nssv2818226, nssv2811462, nssv2813266, nssv2811763, nssv2809280, nssv2814032, nssv2816958, nssv2816399, nssv2812500, nssv2818239, nssv2808970, nssv2818386, nssv2811115, nssv2816116, nssv2814650, nssv2814974, nssv2813396, nssv2808505, nssv2810278, nssv2815495, nssv2809679, nssv2818315, nssv2817781, nssv2811618, nssv2814394, nssv2809615, nssv2809600, nssv2815266, nssv2814319, nssv2809550, nssv2816448, nssv2811285
SamplesNA18508, NA18980, NA19145, NA18603, NA19092, NA21717, NA21301, NA18870, NA21522, NA18510, NA19127, NA18940, NA18519, NA19201, NA18860, NA19131, NA19197, NA18498, NA21391, NA18874, NA18868, NA19137, NA19128, NA19189, NA19239, NA18908, NA21344, NA18867, NA21494, NA19247, NA19210, NA19194, NA19161, NA18933, NA18956, NA21366, NA19202, NA21441, NA19177, NA18518, NA19181, NA19252, NA18523, NA19160, NA19132, NA21309, NA21302, NA19094, NA19183, NA19149, NA19147, NA18517, NA19144, NA21718, NA19193, NA18869, NA19182, NA19178, NA19211, NA18994, NA21486, NA19116, NA21303, NA18852, NA19129, NA19148, NA21440, NA19214
Known GenesSNRPN
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nsv514772
Frequency
Sample Size2366
Observed Gain0
Observed Loss68
Observed Complex0
Frequencyn/a


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