A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv636e199



Internal ID20123938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35169042..35175489hg38UCSC Ensembl
chr19:35659945..35666392hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg386448
hg196448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2656580, esv2670879
SamplesHG00626, HG00650, HG00592, NA20529, NA20543, NA19055, HG00608, NA12286, NA20508, NA19466, HG00559, HG00524, NA12273, HG00100, NA18561, HG01389, HG01374, NA18999, NA18603, HG00103, NA18545, NA12004, NA20332, NA18606, HG00737, HG00654, NA18526, HG00693, NA18988, NA18627, NA12413, HG00327, NA12813, HG00663, NA18967, NA19068, NA19381, NA19379, NA18940, HG00589, HG00501, NA19382, HG00702, HG00448, HG01168, NA19723, NA18982, NA20795, NA12891, HG00634, NA18618, HG00736, HG00610, NA18574, NA19088, HG00247, NA19054, HG00334, HG00537, NA19079, NA18611, HG00512, NA19651, HG00683, NA20775, NA20812, NA18977, NA11932, NA18560, NA11994, HG00705, HG00182, NA19002, HG00427, NA19189, HG00637, HG00159, NA18557, HG00530, NA19789, NA18638, NA18614, NA18613, HG00629, HG00443, NA19082, NA19056, HG00145, NA12003, NA12878, HG00190, NA20809, HG00701, HG00436, HG00533, NA18976, NA18948, NA12234, HG00708, HG00692, NA18566, HG00273, NA19084, HG00404, HG00479, NA20581, HG01197, NA11894, NA18532, HG00117, HG00613, HG00525, NA19099, HG00276, HG00704, NA19682, NA12778, NA18570, HG01107, NA19675, NA18546, NA20296, NA19401, NA19003, NA20801, NA18533, HG01190, HG00265, NA18952, NA18543, NA18559, NA19749, HG00565, NA18628, HG00357, NA18941, NA19773, NA07051, HG01174, HG00473, NA19679, HG01137, HG00116, NA19083, NA07037, NA12763, NA18615, NA18610, HG00620, HG00672, HG01491, HG00312, NA20582, NA19060, NA18987, HG00656, NA12830, HG00310, HG00698, NA19080, NA20528, NA18552, HG00252, HG00472, NA07056, HG01111, NA12890, NA18623, NA19063, NA19065, HG00554, NA18549, NA18622, NA18965, NA18577, NA20509, HG00593
Known GenesFXYD5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv636e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss177
Observed Complex0
Frequencyn/a


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