A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573758



Internal ID16361167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89830015..89831943hg38UCSC Ensembl
Innerchr16:89896423..89898351hg19UCSC Ensembl
Innerchr16:88423924..88425852hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg381929
hg191929
hg181929
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5327n54
Supporting Variantsnssv863481, nssv863488, nssv863474, nssv863451, nssv863421, nssv863441, nssv863453, nssv863497, nssv863491, nssv863464, nssv863416, nssv863500, nssv863429, nssv863426, nssv863444, nssv863465, nssv863431, nssv863495, nssv863473, nssv863422, nssv863505, nssv863463, nssv863493, nssv863498, nssv863461, nssv863509, nssv863427, nssv863462, nssv863466, nssv863459, nssv863423, nssv863472, nssv863442, nssv863419, nssv863471, nssv863492, nssv863454, nssv863439, nssv863480, nssv863432, nssv863450, nssv863487, nssv863468, nssv863446, nssv863438, nssv863484, nssv863435, nssv863467, nssv863510, nssv863447, nssv863506, nssv863456, nssv863457, nssv863411, nssv863494, nssv863434, nssv863420, nssv863508, nssv863424, nssv863501, nssv863496, nssv863475, nssv863503, nssv863436, nssv863485, nssv863433, nssv863483, nssv863477, nssv863415, nssv863413, nssv863478, nssv863448, nssv863452, nssv863482, nssv863410, nssv863414, nssv863479, nssv863469, nssv863460, nssv863470, nssv863425, nssv863458, nssv863502, nssv863507, nssv863476, nssv863412, nssv863428, nssv863443, nssv863437, nssv863418, nssv863417, nssv863499, nssv863449, nssv863440, nssv863430, nssv863489, nssv863486, nssv863490, nssv863445, nssv863455, nssv863504
Samples
Known GenesSPIRE2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573758
Frequency
Sample Size17421
Observed Gain0
Observed Loss101
Observed Complex0
Frequencyn/a


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