A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606322



Internal ID16047045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:16133386..16134327hg38UCSC Ensembl
Innerchr7:16173011..16173952hg19UCSC Ensembl
Innerchr7:16139536..16140477hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38942
hg19942
hg18942
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11222n54
Supporting Variantsnssv1079582, nssv1079544, nssv1079514, nssv1079495, nssv1079487, nssv1079470, nssv1079538, nssv1079563, nssv1079491, nssv1079543, nssv1079511, nssv1079490, nssv1079567, nssv1079557, nssv1079492, nssv1079555, nssv1079520, nssv1079549, nssv1079552, nssv1079572, nssv1079506, nssv1079502, nssv1079482, nssv1079574, nssv1079480, nssv1079494, nssv1079535, nssv1079562, nssv1079521, nssv1079550, nssv1079539, nssv1079556, nssv1079589, nssv1079505, nssv1079498, nssv1079554, nssv1079522, nssv1079558, nssv1079542, nssv1079517, nssv1079573, nssv1079471, nssv1079569, nssv1079532, nssv1079581, nssv1079551, nssv1079476, nssv1079537, nssv1079584, nssv1079570, nssv1079566, nssv1079564, nssv1079485, nssv1079561, nssv1079513, nssv1079515, nssv1079479, nssv1079526, nssv1079583, nssv1079474, nssv1079523, nssv1079579, nssv1079530, nssv1079571, nssv1079553, nssv1079478, nssv1079546, nssv1079540, nssv1079497, nssv1079493, nssv1079473, nssv1079568, nssv1079533, nssv1079484, nssv1079483, nssv1079481, nssv1079560, nssv1079548, nssv1079576, nssv1079529, nssv1079575, nssv1079499, nssv1079565, nssv1079472, nssv1079477, nssv1079527, nssv1079525, nssv1079524, nssv1079580, nssv1079585, nssv1079489, nssv1079504, nssv1079577, nssv1079547, nssv1079545, nssv1079587, nssv1079588, nssv1079586, nssv1079488, nssv1079486, nssv1079536, nssv1079534, nssv1079516, nssv1079508, nssv1079501, nssv1079518, nssv1079507, nssv1079578, nssv1079500, nssv1079512, nssv1079531, nssv1079510, nssv1079503, nssv1079496, nssv1079559, nssv1079528, nssv1079509, nssv1079541, nssv1079519, nssv1079475
Samples
Known GenesISPD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606322
Frequency
Sample Size17421
Observed Gain0
Observed Loss120
Observed Complex0
Frequencyn/a


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