A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv514191



Internal ID15465883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:189646285..189820797hg38UCSC Ensembl
Innerchr3:189364074..189538586hg19UCSC Ensembl
Innerchr3:190846768..191021280hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38174513
hg19174513
hg18174513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2895266, nssv2895225, nssv2895200, nssv2895149, nssv2895211, nssv2895251, nssv2895294, nssv2895217, nssv2895213, nssv2895205, nssv2895192, nssv2895165, nssv2895155, nssv2895290, nssv2895289, nssv2895223, nssv2895179, nssv2895281, nssv2895182, nssv2895170, nssv2895216, nssv2895156, nssv2895161, nssv2895221, nssv2895298, nssv2895279, nssv2895234, nssv2895287, nssv2895208, nssv2895176, nssv2895160, nssv2895236, nssv2895306, nssv2895248, nssv2895246, nssv2895202, nssv2895244, nssv2895171, nssv2895271, nssv2895191, nssv2895166, nssv2895215, nssv2895163, nssv2895226, nssv2895210, nssv2895305, nssv2895280, nssv2895262, nssv2895273, nssv2895190, nssv2895230, nssv2895259, nssv2895186, nssv2895257, nssv2895207, nssv2895158, nssv2895261, nssv2895212, nssv2895242, nssv2895302, nssv2895275, nssv2895253, nssv2895258, nssv2895219, nssv2895285, nssv2895269, nssv2895189, nssv2895222, nssv2895187, nssv2895198, nssv2895308, nssv2895174, nssv2895206, nssv2895307, nssv2895227, nssv2895204, nssv2895303, nssv2895162, nssv2895291, nssv2895247, nssv2895185, nssv2895288, nssv2895153, nssv2895228, nssv2895168, nssv2895295, nssv2895229, nssv2895304, nssv2895274, nssv2895243, nssv2895292, nssv2895178, nssv2895252, nssv2895233, nssv2895263, nssv2895209, nssv2895177, nssv2895218, nssv2895152, nssv2895214, nssv2895256, nssv2895220, nssv2895195, nssv2895188, nssv2895284, nssv2895267, nssv2895239, nssv2895265, nssv2895150, nssv2895293, nssv2895282, nssv2895268, nssv2895283, nssv2895297, nssv2895241, nssv2895159, nssv2895232, nssv2895240, nssv2895164, nssv2895154, nssv2895175, nssv2895183, nssv2895238, nssv2895194, nssv2895254, nssv2895296, nssv2895286, nssv2895260, nssv2895250, nssv2895245, nssv2895224, nssv2895193, nssv2895300, nssv2895172, nssv2895309, nssv2895299, nssv2895270, nssv2895277, nssv2895201, nssv2895169, nssv2895278, nssv2895181, nssv2895237, nssv2895180, nssv2895276, nssv2895157, nssv2895264, nssv2895199, nssv2895272, nssv2895203, nssv2895255, nssv2895151, nssv2895167, nssv2895301, nssv2895235, nssv2895249, nssv2895173, nssv2895197, nssv2895196, nssv2895184, nssv2895231
SamplesNA18998, NA19237, NA19141, NA21636, NA12842, NA18947, NA19249, NA10845, NA18592, NA18508, NA19122, NA18935, NA18507, NA18999, NA18917, NA18603, NA12045, NA19092, NA18545, NA18504, NA12340, NA18959, NA12832, NA19190, NA18633, NA21522, NA12399, NA18969, NA18967, NA18563, NA19005, NA18940, NA19201, NA21359, NA18995, NA19191, NA19119, NA18635, NA19198, NA18558, NA18547, NA18942, NA21479, NA19197, NA18571, NA19138, NA18949, NA18611, NA18970, NA12274, NA18868, NA21512, NA21454, NA21716, NA18990, NA19239, NA19209, NA21634, NA18975, NA21400, NA21599, NA21480, NA21313, NA19210, NA12753, NA10836, NA19175, NA19152, NA19161, NA18933, NA19184, NA19236, NA18516, NA12877, NA18637, NA18579, NA18910, NA18503, NA19221, NA18907, NA18537, NA18566, NA18573, NA19114, NA19177, NA19142, NA19118, NA19000, NA12386, NA12829, NA19181, NA19151, NA18856, NA12249, NA19154, NA18857, NA12827, NA12264, NA19099, NA12817, NA10852, NA18555, NA19252, NA19225, NA21583, NA19160, NA18570, NA19012, NA18974, NA18576, NA18608, NA21608, NA18953, NA18978, NA18632, NA19183, NA19115, NA19108, NA18961, NA19149, NA18564, NA12272, NA19174, NA12873, NA18992, NA21615, NA21390, NA12763, NA21513, NA18911, NA18594, NA19117, NA18501, NA19109, NA19248, NA21404, NA19223, NA18987, NA19211, NA18994, NA18500, NA18609, NA18506, NA18873, NA21614, NA21486, NA19096, NA18854, NA21455, NA21312, NA18852, NA18968, NA12890, NA21487, NA18511, NA21514, NA18612, NA18622, NA19153, NA18620, NA18997
Known GenesTP63
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nsv514191
Frequency
Sample Size2366
Observed Gain0
Observed Loss161
Observed Complex0
Frequencyn/a


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