A curated catalogue of human genomic structural variation

Variant Details

Variant: nsv579520

Internal ID16020243
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:39894900..39895104hg38UCSC Ensembl
Innerchr19:40385540..40385744hg19UCSC Ensembl
Innerchr19:45077380..45077584hg18UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv899356, nssv899351, nssv899375, nssv899369, nssv899286, nssv899360, nssv899344, nssv899278, nssv899326, nssv899361, nssv899358, nssv899355, nssv899362, nssv899334, nssv899325, nssv899317, nssv899319, nssv899353, nssv899352, nssv899380, nssv899303, nssv899379, nssv899335, nssv899341, nssv899306, nssv899322, nssv899329, nssv899302, nssv899338, nssv899323, nssv899324, nssv899309, nssv899310, nssv899307, nssv899280, nssv899284, nssv899274, nssv899320, nssv899282, nssv899279, nssv899296, nssv899304, nssv899370, nssv899308, nssv899367, nssv899347, nssv899292, nssv899372, nssv899333, nssv899283, nssv899330, nssv899277, nssv899314, nssv899273, nssv899311, nssv899299, nssv899378, nssv899313, nssv899365, nssv899340, nssv899357, nssv899363, nssv899377, nssv899337, nssv899359, nssv899332, nssv899281, nssv899291, nssv899381, nssv899316, nssv899315, nssv899294, nssv899371, nssv899343, nssv899339, nssv899298, nssv899327, nssv899305, nssv899297, nssv899290, nssv899285, nssv899368, nssv899275, nssv899354, nssv899376, nssv899287, nssv899350, nssv899295, nssv899373, nssv899366, nssv899364, nssv899374, nssv899301, nssv899288, nssv899342, nssv899276, nssv899348, nssv899382, nssv899293, nssv899318, nssv899312, nssv899331, nssv899321, nssv899336, nssv899346, nssv899349, nssv899345, nssv899328, nssv899300, nssv899289
Known GenesFCGBP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Pubmed ID21841781
Accession Number(s)nsv579520
Sample Size17421
Observed Gain0
Observed Loss110
Observed Complex0

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