A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1301e199



Internal ID22759074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:107492590..107494135hg38UCSC Ensembl
chr8:108504818..108506363hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg381546
hg191546
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2657528, esv2673128
SamplesNA18502, NA20761, NA12842, NA19055, HG00536, NA19664, NA19466, NA18980, HG01389, HG01465, NA19777, NA18616, HG01518, HG00177, NA19443, NA20806, NA19067, NA19746, HG00251, NA20589, HG01351, NA18558, HG00610, NA18574, HG00247, NA20336, HG00243, NA20291, NA19079, NA19651, HG01067, HG00683, HG00106, NA19137, NA19371, HG00705, NA19725, NA18985, HG01133, NA20533, NA18908, NA19007, NA12777, HG00731, HG00557, NA19077, HG00428, HG00732, HG00653, NA19236, HG00344, HG01498, NA19788, NA18579, NA18871, HG01149, NA18534, NA19776, NA18981, HG00740, HG01047, NA18566, HG00651, HG01197, NA18499, NA19453, HG00525, NA12827, HG01334, NA19009, NA18858, NA18593, NA19012, NA12043, NA18608, HG00124, HG00336, NA18961, NA18559, NA19434, HG00375, HG00638, HG00278, NA07051, NA20785, NA19010, NA19470, NA19085, NA18615, NA06986, NA19078, NA19060, NA12749, NA20334, NA19080, NA19711, HG01377, NA18984, NA18989, NA12006, NA19065, NA19074, HG00553
Known GenesANGPT1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1301e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss103
Observed Complex0
Frequencyn/a


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