A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552426



Internal ID16339835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:131111671..131114439hg38UCSC Ensembl
Innerchr10:132909934..132912702hg19UCSC Ensembl
Innerchr10:132799924..132802692hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg382769
hg192769
hg182769
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1443n54
Supporting Variantsnssv761511, nssv761501, nssv761534, nssv761549, nssv761499, nssv761520, nssv761509, nssv761561, nssv761496, nssv761584, nssv761513, nssv761600, nssv761538, nssv761497, nssv761597, nssv761507, nssv761519, nssv761578, nssv761514, nssv761548, nssv761487, nssv761562, nssv761485, nssv761555, nssv761539, nssv761546, nssv761593, nssv761587, nssv761522, nssv761537, nssv761595, nssv761556, nssv761545, nssv761503, nssv761478, nssv761536, nssv761500, nssv761567, nssv761589, nssv761565, nssv761535, nssv761508, nssv761518, nssv761599, nssv761581, nssv761523, nssv761569, nssv761558, nssv761510, nssv761540, nssv761528, nssv761480, nssv761553, nssv761483, nssv761583, nssv761582, nssv761498, nssv761564, nssv761532, nssv761544, nssv761554, nssv761594, nssv761486, nssv761476, nssv761572, nssv761477, nssv761505, nssv761516, nssv761475, nssv761530, nssv761541, nssv761590, nssv761591, nssv761521, nssv761598, nssv761526, nssv761525, nssv761517, nssv761527, nssv761506, nssv761568, nssv761482, nssv761566, nssv761557, nssv761488, nssv761560, nssv761529, nssv761491, nssv761489, nssv761552, nssv761492, nssv761592, nssv761579, nssv761580, nssv761531, nssv761512, nssv761494, nssv761495, nssv761543, nssv761571, nssv761474, nssv761493, nssv761533, nssv761588, nssv761559, nssv761504, nssv761479, nssv761585, nssv761573, nssv761542, nssv761481, nssv761586, nssv761576, nssv761484, nssv761575, nssv761502, nssv761577, nssv761596, nssv761551, nssv761550, nssv761524, nssv761563, nssv761547, nssv761570, nssv761490, nssv761515, nssv761574
Samples
Known GenesTCERG1L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552426
Frequency
Sample Size17421
Observed Gain0
Observed Loss127
Observed Complex0
Frequencyn/a


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