A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602412



Internal ID16389821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32521954..32522114hg38UCSC Ensembl
Innerchr6:32489731..32489891hg19UCSC Ensembl
Innerchr6:32597709..32597869hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38161
hg19161
hg18161
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1055502, nssv1055444, nssv1055504, nssv1055451, nssv1055458, nssv1055480, nssv1055461, nssv1055448, nssv1055494, nssv1055450, nssv1055457, nssv1055488, nssv1055469, nssv1055474, nssv1055454, nssv1055464, nssv1055436, nssv1055462, nssv1055483, nssv1055441, nssv1055435, nssv1055438, nssv1055478, nssv1055472, nssv1055477, nssv1055453, nssv1055479, nssv1055449, nssv1055501, nssv1055460, nssv1055459, nssv1055463, nssv1055491, nssv1055445, nssv1055497, nssv1055509, nssv1055508, nssv1055452, nssv1055468, nssv1055475, nssv1055470, nssv1055427, nssv1055482, nssv1055500, nssv1055431, nssv1055425, nssv1055487, nssv1055443, nssv1055430, nssv1055498, nssv1055466, nssv1055490, nssv1055492, nssv1055481, nssv1055447, nssv1055456, nssv1055506, nssv1055473, nssv1055428, nssv1055426, nssv1055503, nssv1055495, nssv1055446, nssv1055493, nssv1055496, nssv1055467, nssv1055432, nssv1055486, nssv1055439, nssv1055471, nssv1055476, nssv1055440, nssv1055507, nssv1055484, nssv1055485, nssv1055433, nssv1055489, nssv1055429, nssv1055505, nssv1055499, nssv1055455, nssv1055434, nssv1055465, nssv1055437, nssv1055442
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602412
Frequency
Sample Size17421
Observed Gain0
Observed Loss85
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer